Subject Index

AB C DEF GHI JKL MNO PQRS TUV WXYZ

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Chapters in boldface indicate a major discussion of a topic.

Please also note that due to the impressive size of this index it was necessary to break it down in to smaller groups. The Alphabet above will take you to any letter you please and the grouping of letters is indicated by spaces between the letters.

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Subject Index P
Pachymeningitis, (Clinical Volume 2, Chapter 5) 
4p addition syndrome, (Foundations Volume 3, Chapter 52) 
11p addition syndrome, (Foundations Volume 3, Chapter 52) 
20p addition syndrome, (Foundations Volume 3, Chapter 52) 
Paddleball, eye injuries from, protective device effectiveness and, (Clinical Volume 5, Chapter 45) 
Paddle sports, eye injuries from, protective device effectiveness and, (Clinical Volume 5, Chapter 45) 
Paecilomyces lilacnus, endophthalmitis, (Clinical Volume 4, Chapter 55) 
PAF. See Platelet-activating factor
Page amoeba saline, (Foundations Volume 2, Chapter 40) 
Paget disease
angioid streaks and, (Clinical Volume 3, Chapter 36) 
Pain. See also Anesthetics; Neuralgia
in Acanthamoeba keratitis, (Clinical Volume 4, Chapter 18A) 
in carotid aneurysms, intracavernous, (Clinical Volume 2, Chapter 17) 
in communicating artery aneurysm, posterior, (Clinical Volume 2, Chapter 17) 
corneal sensitivity to, (Foundations Volume 2, Chapter 4) 
facial. (See Facial pain)
facial nerve blocks, (Clinical Volume 6, Chapter 1) 
in glaucoma, acute angle-closure, (Clinical Volume 3, Chapter 53) 
headache. (See Headaches)
in lacrimal gland disorders, (Clinical Volume 2, Chapter 40) 
in neuro-ophthalmologic case history, (Clinical Volume 2, Chapter 1) 
ophthalmoplegias. (See Ophthalmoplegia, painfulin)
in optic neuritis, (Clinical Volume 2, Chapter 5) 
orbital disease and, (Clinical Volume 2, Chapter 22) 
postoperative, in children, (Clinical Volume 6, Chapter 81) 
referred, orbital, (Clinical Volume 2, Chapter 29) 
sensory innervation of globe and, (Clinical Volume 2, Chapter 3) 
and visual loss, (Clinical Volume 2, Chapter 1) 
Paintball, eye injuries from, protective device effectiveness and, (Clinical Volume 5, Chapter 45) 
Painted lenses, therapeutic uses of, (Clinical Volume 1, Chapter 56) 
Palinopsic polyopia, (Foundations Volume 2, Chapter 22) 
Palisading necrobiotic granuloma, (Clinical Volume 2, Chapter 39) 
Pallor
optic disc. (See Optic disc, pallorof)
retinopathy of blood dyscrasias and, (Clinical Volume 3, Chapter 18) 
Palpation, in intraocular pressure estimation, (Foundations Volume 2, Chapter 7) 
Palpebral arcades, (Foundations Volume 1, Chapter 5) 
Palpebral creases, (Foundations Volume 1, Chapter 5) 
Palpebral fissures, in craniofacial syndromes, (Clinical Volume 6, Chapter 110) 
Palpebral lobe of lacrimal gland, (Clinical Volume 2, Chapter 40) 
pleomorphic adenoma involving, (Clinical Volume 2, Chapter 40) 
Palpebral-oculogyric reflex, (Clinical Volume 2, Chapter 8) 
Palpebral slant
in Apert’s disease, (Clinical Volume 5, Chapter 29) 
in Hallermann-Streiff syndrome, (Clinical Volume 5, Chapter 29) 
in mandibulofacial dysostosis, (Clinical Volume 5, Chapter 29) 
Palpebral vernal keratoconjunctivitis, 2–4, (Clinical Volume 4, Chapter 9) 
PALs. See Progressive addition lenses (PALs)
Palsy. See also Paralysis
of cranial nerves, (Clinical Volume 1, Chapter 19)  (Clinical Volume 2, Chapter 29) See also Gaze, Ophthalmoplegia, palsies, specific nerves
Bell’s phenomenon and, (Clinical Volume 1, Chapter 2) 
bulbar, congenital. (See Mobius syndrome)
facial. (See Bell’s palsy; Facial nerve, paralysis)
in Paget’s disease, (Clinical Volume 5, Chapter 29) 
saccadic, congenital, (Clinical Volume 2, Chapter 10) 
vertical deviation in, (Clinical Volume 2, Chapter 12) 
facial nerve, traumatic, (Foundations Volume 1, Chapter 37) 
oculomotor nerve, tonic pupil versus, (Foundations Volume 2, Chapter 9) 
superior oblique, congenital, (Foundations Volume 3, Chapter 59) 
Pancoast superior sulcus syndrome, (Clinical Volume 2, Chapter 15) 
Pancreas, fibrocystic disease of, (Clinical Volume 5, Chapter 24) 
Pancreatic disease
acute pancreatitis, retinopathy in, (Clinical Volume 5, Chapter 30) 
vitamin A deficiency and, (Clinical Volume 5, Chapter 30) 
Pancreatitis, retinopathy in, (Clinical Volume 5, Chapter 30) 
PANDO (primary acquired nasolacrimal duct obstruction), (Clinical Volume 4, Chapter 13) 
Panniculitis, orbit in, (Clinical Volume 2, Chapter 35) 
Pannus, (Clinical Volume 6, Chapter 28) 
in giant papillary conjunctivitis, 2, (Clinical Volume 4, Chapter 9A) 
phlyctenular, chronic inferior, (Clinical Volume 4, Chapter 8) 
Panocular vascular insufficiency, (Foundations Volume 3, Chapter 13) 
Panophthalmitis, (Foundations Volume 3, Chapter 3) See also Endophthalmitis
Panretinal photocoagulation
in diabetes mellitus, (Foundations Volume 3, Chapter 18) 
retinal blood flow effects, (Foundations Volume 2, Chapter 5) 
Pantoscopic angle (tilt), (Clinical Volume 1, Chapter 42) 
of aspheric spectacle lenses, (Clinical Volume 1, Chapter 50) 
Papanicolaou technique, (Clinical Volume 4, Chapter 35) 
Papaverine, effect on ocular blood flow, (Foundations Volume 2, Chapter 5) 
Papilla, (Clinical Volume 2, Chapter 4) 
conjunctival. (See also Giant papillary conjunctivitis (GPC))
optic nerve. (See Optic discof)
traction, vitrectomy in, (Clinical Volume 6, Chapter 56) 
Papilledema, (Clinical Volume 2, Chapter 5)  (Foundations Volume 3, Chapter 16) See also Disc swelling; Edema, optic nerve
in Apert’s disease, (Clinical Volume 5, Chapter 29) 
chorioretinal folds caused by, (Clinical Volume 3, Chapter 36) 
clinical features, (Clinical Volume 2, Chapter 5) 
fully developed, (Clinical Volume 2, Chapter 5) 
in Hunter’s syndrome, (Clinical Volume 2, Chapter 5) 
in Maroteaux-Lamy syndrome, (Foundations Volume 3, Chapter 54B) 
in mucopolysaccharidoses, (Clinical Volume 2, Chapter 5) 
in optic nerve glioma, (Clinical Volume 2, Chapter 42) 
in pachymeningitis, (Clinical Volume 2, Chapter 5) 
pseudopapilledema, (Clinical Volume 2, Chapter 5) 
in juvenile diabetes, (Clinical Volume 2, Chapter 5) 
in pseudotumor cerebri, (Clinical Volume 2, Chapter 5) 
Papillitis, (Clinical Volume 2, Chapter 5) See also Optic neuritis; Papilledema; (Foundations Volume 3, Chapter 16) 
chorioretinal folds caused by, (Clinical Volume 3, Chapter 36) 
Papillomavirus. See Human papillomavirus (HPV)
Papillopathy
ischemic, after cataract extraction, (Clinical Volume 2, Chapter 5) 
radiation-induced, (Clinical Volume 3, Chapter 36A) 
Papillophlebitis, (Clinical Volume 2, Chapter 5) (Clinical Volume 4, Chapter 44) See also Retinal vasculitis
in retinal vein occlusion, central, (Clinical Volume 3, Chapter 15) 
Papillorenal syndrome, (Clinical Volume 5, Chapter 31) 
Papular angiofibroma, in tuberous sclerosis, (Clinical Volume 3, Chapter 34) 
Papulosis, malignant atrophic, (Clinical Volume 5, Chapter 27) 
Parabulbar (sub-Tenon) anesthesia, (Clinical Volume 6, Chapter 1) 
Paracentesis
anterior chamber, during scleral buckling, (Clinical Volume 6, Chapter 59) 
in chemical injuries, (Clinical Volume 4, Chapter 28) 
glaucoma surgery and, (Clinical Volume 6, Chapter 15) 
in traumatic hyphema, (Clinical Volume 6, Chapter 39) 
Paracentral nerve fiber bundle defects, (Clinical Volume 3, Chapter 49) 
Paracentral scotoma, hemianopic, (Foundations Volume 2, Chapter 22) 
Paraflocculus, ventral, ocular motility and, (Foundations Volume 2, Chapter 23) 
Paraganglioma
histologic features, (Clinical Volume 2, Chapter 41) 
Parageusia, in Bell palsy, (Foundations Volume 1, Chapter 37) 
Parainfluenzavirus, (Foundations Volume 2, Chapter 85) 
Paraldehyde, ocular toxicity, (Clinical Volume 5, Chapter 37) 
Parallel visual pathways, (Clinical Volume 2, Chapter 2) (Clinical Volume 2, Chapter 10) 
magnocellular, parvocellular parallel pathway, (Clinical Volume 2, Chapter 10) 
Paralysis. See also Palsy, of cranial nerves
of accommodation, (Clinical Volume 2, Chapter 15) 
horizontal gaze, psychogenic, (Clinical Volume 2, Chapter 10) 
Landry’s ascending. (See Guillain-Barre syndrome, bulbar variant)
psychic, of gaze, (Clinical Volume 2, Chapter 7) 
Paralytic ectropion, (Clinical Volume 5, Chapter 73) 
Paramedian pontine reticular formation. See Pontine paramedian reticular formation
Paramethadione
Paramethasone, ocular toxicity, (Clinical Volume 5, Chapter 37) 
Paramyxoviruses, (Clinical Volume 4, Chapter 7) 
Paranasal sinuses
cancer, orbital extension, (Clinical Volume 2, Chapter 46) 
diseases
and optic neuritis, (Clinical Volume 2, Chapter 5) 
infection. (See Sinusitis)
mucoceles, (Clinical Volume 2, Chapter 6) (Clinical Volume 2, Chapter 31) See also Mucoceles, of paranasal sinuses
tumors
optic nerve and, (Clinical Volume 2, Chapter 5) 
orbital involvement, (Clinical Volume 2, Chapter 24) 
in Wegener’s granulomatosis, (Clinical Volume 2, Chapter 35) 
Paraneoplastic autoimmune demyelination, (Clinical Volume 2, Chapter 6) 
Paraneoplastic optic neuritis, (Clinical Volume 2, Chapter 5) 
Paraneoplastic pemphigus, (Clinical Volume 4, Chapter 2) 
Paraneoplastic syndromes, metastatic cancer to, (Clinical Volume 5, Chapter 34) 
Paraproteinemias, multiple myeloma, (Clinical Volume 4, Chapter 15) 
Parasite, onchocerciasis and, (Clinical Volume 5, Chapter 62) 
Parasites
Parasitic diseases, (Clinical Volume 5, Chapter 33) See also speicific disease
laboratory diagnosis, (Clinical Volume 4, Chapter 1) 
polymerase chain reaction in, (Clinical Volume 4, Chapter 1) 
rickettsial. (See Rickettsial diseases)
Parasympathetic agents (miotics), intraocular pressure and, (Foundations Volume 2, Chapter 7) 
Parasympathetic nerves, stimulation of protein secretion by, (Foundations Volume 2, Chapter 2A) 
Parasympathetic system
and darkness reflex, (Foundations Volume 2, Chapter 9) 
drugs affecting, pupillary effects of, (Foundations Volume 2, Chapter 9 ) 
growth and regeneration in, (Foundations Volume 2, Chapter 9) 
intraocular pressure and, (Foundations Volume 2, Chapter 7) 
Parasympathomimetic agents, (Clinical Volume 3, Chapter 56) See also Miotics
Parasympathomimetics, systemic toxicity, (Clinical Volume 5, Chapter 37) 
Parathyroid disorders, (Clinical Volume 5, Chapter 21 ) 
hyperparathyroidism, (Clinical Volume 5, Chapter 21) 
hypoparathyroidism, (Clinical Volume 5, Chapter 21) 
Paratrigeminal neuralgia, (Foundations Volume 1, Chapter 36) 
Paraxial rays, (Clinical Volume 1, Chapter 30) (Clinical Volume 1, Chapter 33) 
and paraxial power of spherical surface, (Clinical Volume 1, Chapter 30) 
Paresis. (See Palsy, of cranial nerves)
Paredrine. (hydroxyamphetamine) in test for oculosympathetic paresis, (Clinical Volume 2, Chapter 15) See Hydroxyamphetamine
Paresis
vertical gaze, Niemann-Pick disease and, (Foundations Volume 3, Chapter 54B) 
Pareto, Vilfredo, (Clinical Volume 5, Chapter 69) 
Pargyline (Eutonyl)
effect on aqueous humor, (Foundations Volume 3, Chapter 29) 
Parietal eye fields, ocular motility and, (Foundations Volume 1, Chapter 38) (Foundations Volume 2, Chapter 23) 
Parietal lobe
optic radiation, lesions, (Clinical Volume 2, Chapter 7) 
in saccade generation, (Clinical Volume 2, Chapter 10) 
Parieto-occipital artery, (Clinical Volume 2, Chapter 4) 
Parieto-occipital-temporal junction, (Clinical Volume 1, Chapter 4) 
Parinaud dorsal midbrain syndrome
accommodation in, (Clinical Volume 2, Chapter 15) 
eye movements in, (Clinical Volume 2, Chapter 12) 
lid retraction in, (Clinical Volume 2, Chapter 3) 
Parinaud-plus syndrome, (Clinical Volume 2, Chapter 12) 
Parkinson disease
progressive supranuclear palsy versus, (Clinical Volume 2, Chapter 10) 
Parkinsonian disorders, (Clinical Volume 2, Chapter 10) 
Parkinson syndrome, (Clinical Volume 2, Chapter 15) 
Parks three-step test, in dissociated strabismus complex, (Clinical Volume 1, Chapter 18) 
Paromomycin
in Acanthamoeba keratitis, (Foundations Volume 2, Chapter 66) 
Paroocellular lateral geniculate nucleus layers, (Clinical Volume 2, Chapter 4) 
Paroxysmal hemicrania, (Clinical Volume 2, Chapter 16) 
PAR (posterior apical radius), (Clinical Volume 1, Chapter 55) 
Parry-Romberg syndrome (progressive hemifacial atrophy), (Foundations Volume 1, Chapter 37) 
Pars plana, (Foundations Volume 1, Chapter 13) 
nonpigmented epithelial cells of, (Foundations Volume 1, Chapter 13) 
ultrasound biomicroscopy through, (Foundations Volume 2, Chapter 106) 
vitrectomy, (Clinical Volume 6, Chapter 66) See also Vitrectomy
Pars plana approach, in anterior chamber paracentesis, (Clinical Volume 6, Chapter 59) 
Pars plana vitrectomy, for central retinal vein occlusion, (Clinical Volume 3, Chapter 15) 
Partial deletion syndromes, (Foundations Volume 3, Chapter 52) 
Partial trisomy syndromes, (Foundations Volume 3, Chapter 52) 
Participation
direct assessment, (Clinical Volume 5, Chapter 51) 
Particle size, oral medications and, bioinequivalence and, (Foundations Volume 3, Chapter 22) 
Parvocellular lateral geniculate nucleus, (Foundations Volume 2, Chapter 19) 
Pasteurella multocida, (Clinical Volume 4, Chapter 4) 
Past-pointing, in vestibular disorders, (Clinical Volume 2, Chapter 11) 
Patch graft
scleral, double-plate shunt placement and, (Clinical Volume 6, Chapter 17) 
Pathologic processes, (Foundations Volume 3, Chapter 1 ) 
Paton lines, in papilledema, (Clinical Volume 2, Chapter 5) 
Pattern discrimination perimetry (PDP), (Foundations Volume 2, Chapter 17) 
Pattern dystrophy(ies), (Clinical Volume 3, Chapter 9) 
benign concentric annular macular dystrophy as, (Clinical Volume 3, Chapter 9) 
butterfly-shaped pigment dystrophy of fovea as, (Clinical Volume 3, Chapter 9) 
dominant slowly progressive macular dystrophy of Singerman-Berkow-Patz as, (Clinical Volume 3, Chapter 9) 
macroreticular dystrophy of retinal pigment epithelium as, (Clinical Volume 3, Chapter 9) 
pigment epithelial dystrophy of Noble-Carr-Siegal as, (Clinical Volume 3, Chapter 9) 
of pigment epithelium of Marmor and Byers, (Clinical Volume 3, Chapter 9) 
Sjorgren’s reticular dystrophy of retinal pigment epithelium as, (Clinical Volume 3, Chapter 9) 
Pattern electroretinography, (Clinical Volume 2, Chapter 10) 
Pattern visual evoked potential (PVEP), (Foundations Volume 2, Chapter 105) 
Pattern visual evoked potentials, (Clinical Volume 2, Chapter 2) 
Paving stone degeneration of retina, (Clinical Volume 3, Chapter 7) (Clinical Volume 3, Chapter 26) 
9p deletion syndrome, (Foundations Volume 3, Chapter 52) 
11p deletion syndrome, (Foundations Volume 3, Chapter 52) 
18p deletion syndrome, (Foundations Volume 3, Chapter 52) 
PDP (pattern discrimination perimetry), (Foundations Volume 2, Chapter 17) 
PE. See Pigment epithelium
Peau d’orange pattern, in angioid streaks, (Clinical Volume 3, Chapter 36) (Clinical Volume 4, Chapter 66) 
PECC (Protective Eyewear Certification Council), (Clinical Volume 5, Chapter 45) 
Pectinate ligament, (Foundations Volume 1, Chapter 1) 
Pediatric migraine, 45
Pediatric neuro-ophthalmology, (Clinical Volume 2, Chapter 13) 
acquired visual loss in childhood, 16–20
blind infant, 9–16
congenital motor anomalies, 20–35
Duane’s retraction syndrome, 21–25
elevator deficiencies, 27–29
Marcus Gunn jaw-winking synkineses, 29–32
Mobius syndrome, 25–27
orbital mechanics, 20–32
restrictive syndromes, 32
Brown tendon sheath syndrome, 32–34
congenital fibrosis syndromes, 34–35
vertical retraction syndrome, 29
functional visual loss, 62–65
headache in children, 44–46
pediatric migraine, 45
pediatric pseudotumor cerebri, 45–46
myasthenia gravis in childhood, 49–50
nystagmus, related disorders, 35–42
congenital nystagmus, 36–38
congenital ocular motor apraxia, 40–41
dyslexia, 42–44
Heimann-Bielschowsky phenomenon, 39–40
latent nystagmus, 38
ocular flutter/opsoclonus, 41–42
periodic alternating nystagmus, 39
spasmus nutans, 41
transient idiopathic nystagmus of infancy, 35
ocular motor cranial neuropathies, 46–49
ocular torticollis, 61–62
patient encounter, (Clinical Volume 2, Chapter 13) 
symptomatic sensory, nonparetic strabismic abnormalities, 50–51
accommodative effort syndrome, 61
convergence insufficiencies, 60–61
esotropia, acquired, 57–59
acute acquired comitant estropia, 57–58
cyclic esotropia, 58–59
divergence insufficiency estropia, 58
progressive estropia with nyopia, 59
failure of fusional mechanisms, 53–57
acquired central defects, 53–55
acquired visual loss, 56–57
congenital anomalies, 55–56
problems at near, 60–61
visual development, 8–9
Pediatric ophthalmology. See also Infants
acquired visual loss in, (Clinical Volume 2, Chapter 13) 
anesthesia in, (Clinical Volume 6, Chapter 81 ) 
surgery and
patient preparation for, (Clinical Volume 6, Chapter 80 ) 
aphakia
epikeratoplasty for, (Clinical Volume 6, Chapter 45) 
optical correction, (Clinical Volume 1, Chapter 45 ) 
cellulitis in, preseptal, nonsuppurative, (Clinical Volume 4, Chapter 25) 
Coats’ disease in, (Clinical Volume 6, Chapter 72) 
common diseases and, (Clinical Volume 6, Chapter 81) 
congenital syndromes in, (Clinical Volume 6, Chapter 81) 
motor and sensory anomalies, (Clinical Volume 2, Chapter 13 ) 
conjunctivitis-otitis syndrome, (Clinical Volume 4, Chapter 5) 
corneal opacities in, surgical management, (Clinical Volume 6, Chapter 106) 
craniopharyngioma in, (Clinical Volume 2, Chapter 6) 
cycloplegic refraction in, (Clinical Volume 1, Chapter 41) 
dermoids in, corneal, (Clinical Volume 6, Chapter 106) 
Ewing’s sarcoma in, metastasis to orbit, (Clinical Volume 2, Chapter 46) 
facial palsies in, (Clinical Volume 2, Chapter 8) 
familial exudative vitreoretinopathy in, (Clinical Volume 6, Chapter 72) 
glaucoma in, congenital, cataracts and, (Clinical Volume 3, Chapter 55) 
health status in, cataract surgery and, (Clinical Volume 6, Chapter 100) 
hypoglycemia, cataract in, (Clinical Volume 5, Chapter 41) 
infectious diseases and, (Clinical Volume 6, Chapter 81) 
intraocular lenses in, (Clinical Volume 1, Chapter 68) 
iridocyclitis in, chronic, (Clinical Volume 4, Chapter 42) 
keratoplasty in
neuroblastoma in. (See also Neuroblastoma)
metastasis to orbit, (Clinical Volume 2, Chapter 46) 
neuro-ophthalmology in, congenital anomalies and, (Clinical Volume 2, Chapter 13 ) 
nutritional blindness, 4, (Clinical Volume 5, Chapter 59) 
ocular trauma, (Clinical Volume 6, Chapter 111) See also Child abuse
oculomotor palsies of, (Clinical Volume 2, Chapter 12) 
abducens, isolated, (Clinical Volume 2, Chapter 12) 
optic atrophies in, heredodegenerative, (Clinical Volume 2, Chapter 5 ) 
optic meningiomas in, (Clinical Volume 2, Chapter 5) 
optic neuritis in, (Clinical Volume 2, Chapter 5) 
acute disseminated encephalomyelitis and, (Clinical Volume 2, Chapter 5) 
primary hyperoxaluria in, (Clinical Volume 5, Chapter 31) 
proptosis in, 2, (Clinical Volume 2, Chapter 14) 
acute, (Clinical Volume 2, Chapter 27) See also Proptosis, acute, childhood
retinal detachment in, (Clinical Volume 6, Chapter 72 ) 
anatomic considerations, (Clinical Volume 6, Chapter 72) 
general considerations, (Clinical Volume 6, Chapter 72) 
retinal dysplasia in, (Clinical Volume 6, Chapter 72) 
retinoblastoma. (See Retinoblastoma)
retinoschisis in, congenital, (Clinical Volume 6, Chapter 72) 
rheumatoid arthritis, juvenile. (See Rheumatoid arthritis, juvenile (Still’s disease))
strabismus in, chemodenervation in, (Clinical Volume 6, Chapter 89) 
surgery in
for corneal opacities, (Clinical Volume 6, Chapter 106 ) 
patient preparation for, (Clinical Volume 6, Chapter 80 ) 
scleral buckling, (Clinical Volume 6, Chapter 72) 
toxic epidermal necrolysis in, (Clinical Volume 5, Chapter 27) 
transient cerebral blindness in, (Clinical Volume 2, Chapter 7) 
tuberculosis, isoniazid prophylaxis, (Clinical Volume 4, Chapter 58) 
xanthogranuloma in. (See Xanthogranuloma, juvenile)
Pediatric pseudotumor cerebri, 45–46
Pedicle flap, subcutaneous, 5, (Clinical Volume 5, Chapter 88) 
Pedicles, photoreceptor, (Clinical Volume 3, Chapter 1) 
Peduncular hallucinations, (Clinical Volume 2, Chapter 7) 
Pel-Ebstein fever, (Clinical Volume 2, Chapter 39) 
Pellucid marginal corneal degeneration, (Clinical Volume 4, Chapter 16) 
videokeratography in, (Clinical Volume 1, Chapter 65) 
Pellucid marginal degeneration, (Foundations Volume 2, Chapter 112) 
Pelota vasca, eye injuries from, protective device effectiveness and, (Clinical Volume 5, Chapter 45) 
Pemphigoid, (Foundations Volume 3, Chapter 8) 
Pemphigus vegetans, (Foundations Volume 2, Chapter 29) 
Penbriten. See Ampicillin
Penciclovir
mechanism of action, (Foundations Volume 3, Chapter 37) 
Penetrance, genetic, defined, (Foundations Volume 3, Chapter 51) 
Penetrating keratoplasty. See Keratoplasty, penetrating
Penetrating trauma. See Trauma, penetrating
Penicillin(s), (Clinical Volume 4, Chapter 26) 
for cellulitis, preseptal, (Foundations Volume 3, Chapter 36) 
for conjunctivitis
in corneal ulcers, (Clinical Volume 4, Chapter 18) 
extended-spectrum, (Clinical Volume 4, Chapter 26) 
G (benzyl), (Clinical Volume 4, Chapter 26) 
fortified topical preparation, (Clinical Volume 4, Chapter 18) 
in gonococcal conjunctivitis, (Clinical Volume 4, Chapter 5) 
in gonococcal conjunctivitis, neonatal, (Clinical Volume 4, Chapter 6) (Clinical Volume 4, Chapter 26) 
hypersensitivity to, (Clinical Volume 4, Chapter 26) 
intravitreal injection, (Clinical Volume 4, Chapter 26) 
Pentagonal repair, of lid coloboma, (Clinical Volume 6, Chapter 110) 
Pentamidine, for pneumocystic choroiditis, (Foundations Volume 2, Chapter 66) 
Penthrane. See Methoxyflurane (Penthrane)
Pentobarbital, ocular toxicity, (Clinical Volume 5, Chapter 37) 
Pentolinium, ocular toxicity, (Clinical Volume 5, Chapter 37) 
Pentoxifylline (Trental), and diabetic retinopathy, (Clinical Volume 3, Chapter 30) 
Peptides. See also specific peptides
vasoactive, effect on ocular blood flow, (Foundations Volume 2, Chapter 5) 
Peptostreptococcus, corneal ulcers, (Clinical Volume 4, Chapter 18) 
Perceptible acuity, minimum, (Clinical Volume 1, Chapter 33) 
Perception, simultaneous, (Clinical Volume 1, Chapter 5) 
Percutaneous inferior orbitotomy, (Clinical Volume 5, Chapter 86) 
Perennial allergic rhinoconjunctivitis, (Clinical Volume 4, Chapter 2) 
Perfluorocarbon liquids
physical properties, (Clinical Volume 6, Chapter 54) 
as vitreous substitutes, (Clinical Volume 6, Chapter 54)  (Clinical Volume 6, Chapter 56 ) 
biocompatibility, (Clinical Volume 6, Chapter 54) 
in giant retinal tears, (Clinical Volume 6, Chapter 54) 
indications and techniques, (Clinical Volume 6, Chapter 54) 
in proliferative vitreoretinopathy, (Clinical Volume 6, Chapter 54) 
Perfluoro-n-octane (Perfluoron), as vitreous substitute, (Clinical Volume 6, Chapter 56) 
Perfluoroperhydrophenanthrene (Vitreon), as vitreous substitute, (Clinical Volume 6, Chapter 56) 
Perfluoropropane, (Clinical Volume 3, Chapter 54E) 
as vitreous substitute, (Clinical Volume 6, Chapter 56) 
Perforating injuries, (Foundations Volume 3, Chapter 6) 
during refractive surgery, (Foundations Volume 3, Chapter 6) 
Perforations
corneal. (See Cornea, perforations)
globe. (See Globe, perforating injury)
scleral
fibrous ingrowth, (Clinical Volume 3, Chapter 7) 
intercalary, spontaneous, (Clinical Volume 4, Chapter 23) 
in scleral buckling surgery, (Clinical Volume 6, Chapter 59) 
Perfusion
in chemical injuries, (Clinical Volume 4, Chapter 28) 
in outflow facility measurement, (Foundations Volume 2, Chapter 7) 
Perfusion pressure. See Blood pressure
PERG. See Pattern electroretinogram (PERG)
Periaqueductal syndrome. See Parinaud’s dorsal midbrain syndrome
Periarteritis nodosa. See Polyarteritis nodosa
Peribulbar anesthesia, (Clinical Volume 6, Chapter 1) 
Pericentral retinitis pigmentosa, (Clinical Volume 3, Chapter 9) 
Perimeter corneal reflex test, (Clinical Volume 1, Chapter 6) 
Perimetry, (Clinical Volume 2, Chapter 2)  (Foundations Volume 2, Chapter 17) See also Automated perimetry
accuracy and reliability, (Clinical Volume 3, Chapter 49 ) 
automated, (Clinical Volume 3, Chapter 49) 
differential light threshold in, (Clinical Volume 3, Chapter 49) 
sensitivity versus, (Clinical Volume 3, Chapter 49) 
FASTPAC full threshold strategy in, (Clinical Volume 2, Chapter 2) (Clinical Volume 3, Chapter 49) 
full-threshold strategy, (Clinical Volume 3, Chapter 49) 
global indices in, (Clinical Volume 3, Chapter 49) 
one-level suprathreshold screen, with quantification of defects, in automated perimetry, (Clinical Volume 3, Chapter 49) 
screening programs, (Clinical Volume 3, Chapter 49) 
single-level suprathreshold test, (Clinical Volume 3, Chapter 49) 
static threshold, (Clinical Volume 2, Chapter 2) 
Swedish interactive threshold algorithm, (Clinical Volume 3, Chapter 49) 
testing strategies, (Clinical Volume 3, Chapter 49) 
two-level suprathreshold test, (Clinical Volume 3, Chapter 49) 
Bebie (cummulative defect) curves in, (Clinical Volume 3, Chapter 49) 
binocular, in monofixation syndrome, (Clinical Volume 1, Chapter 14) 
facial structure and, (Clinical Volume 3, Chapter 49) 
false-negative catch trials in, (Clinical Volume 3, Chapter 49) 
false-positive catch trials in, (Clinical Volume 3, Chapter 49) 
frequency-doubling, (Foundations Volume 2, Chapter 17) 
frequency doubling technology in, (Clinical Volume 3, Chapter 49) 
frequency of seeing curve in, (Clinical Volume 3, Chapter 49) 
global indices in, (Clinical Volume 3, Chapter 49) 
hemifield analysis in, (Clinical Volume 3, Chapter 49) 
high-pass resolution, (Foundations Volume 2, Chapter 17) 
intereye comparisons in, (Clinical Volume 3, Chapter 49) 
learning curve in, (Clinical Volume 3, Chapter 49) 
lens rim artifacts, (Clinical Volume 3, Chapter 49) 
light adaptation and, (Foundations Volume 2, Chapter 16) 
long-term fluctuations and, (Clinical Volume 3, Chapter 49) 
manual. (See Perimetry, Goldmann)
media opacities and, (Clinical Volume 3, Chapter 49) 
neuro-ophthalmologic examination, (Clinical Volume 2, Chapter 10) 
numeric printouts, (Clinical Volume 3, Chapter 49) 
patient variables and, (Clinical Volume 3, Chapter 49) 
point-by-point comparisons in, (Clinical Volume 3, Chapter 49) 
psychologic factors in, (Clinical Volume 3, Chapter 49) 
refractive errors and, (Clinical Volume 3, Chapter 49) 
reliability, assessment, (Clinical Volume 3, Chapter 49) 
small pupils artifact, (Clinical Volume 3, Chapter 49) 
statistical analysis in, (Clinical Volume 3, Chapter 49) 
tangent screen, automated static screening perimetry, (Clinical Volume 2, Chapter 10) 
temporal modulation, (Foundations Volume 2, Chapter 17) 
threshold-related strategy, (Clinical Volume 3, Chapter 49) 
Perimetry testing
neuro-ophthalmologic examination, (Clinical Volume 2, Chapter 10) 
tangent screen, automated static screening perimetry, (Clinical Volume 2, Chapter 10) 
Perinatal infection, cataract with, (Clinical Volume 5, Chapter 41) 
Perineuritis, (Clinical Volume 2, Chapter 5) 
and inflammatory pseudotumor, (Clinical Volume 2, Chapter 27) 
Periocular injections, pharmacokinetics and, (Foundations Volume 3, Chapter 23) 
Periodic acid-Schiff stain, (Foundations Volume 2, Chapter 40) 
Periodic acid-Schiff staining, (Foundations Volume 2, Chapter 40) 
Periodic paralysis, (Clinical Volume 5, Chapter 28) 
Periorbital soft tissue, (Clinical Volume 2, Chapter 21) 
Peripapillary atrophy
in ocular histoplasmosis syndrome, (Clinical Volume 4, Chapter 48) 
Peripapillary capillaries, radial, (Foundations Volume 2, Chapter 5) 
Peripapillary degeneration, chorioretinal, helicoidal, (Clinical Volume 4, Chapter 66) 
Peripheral anterior synechiae as complication of hyphema, (Clinical Volume 4, Chapter 61) 
Peripheral anterior vitritis, (Foundations Volume 1, Chapter 16) 
Peripheral corneal rings, with gastrointestinal diseases, non-Wilsonian chronic liver disease, (Clinical Volume 5, Chapter 30) 
Peripheral field defects, (Foundations Volume 2, Chapter 109) 
Peripheral nerves, histologic composition, 2, (Clinical Volume 2, Chapter 41) 
Peripheral nerve sheath, tumors, (Clinical Volume 2, Chapter 41) 
Peripheral nervous system, Lyme disease affecting, (Foundations Volume 2, Chapter 75) 
Peripheral neurofibromatosis. See Neurofibromatosis
Peripheral proliferative retinopathies, (Foundations Volume 2, Chapter 113C) 
Peripheral scotomata, (Clinical Volume 2, Chapter 7) 
Peripheral streak lesions of fundus, in ocular histoplasmosis, (Clinical Volume 4, Chapter 48) 
Peripheral thinning disorders, (Foundations Volume 2, Chapter 112) 
Peripheral ulcerative keratitis, sterile, associated with collagen vascular disease, (Clinical Volume 4, Chapter 2) 
Peripheral viewing, ophthalmoscopy and, (Clinical Volume 1, Chapter 63) 
Peripherin/RDS, retinal degeneration and, (Clinical Volume 4, Chapter 66) 
Periphlebitis
in pars planitis, (Clinical Volume 4, Chapter 43) 
in phakic patients with cystoid macular edema and vitreous inflammation, (Clinical Volume 4, Chapter 43) 
in retinal vasculitis, (Clinical Volume 2, Chapter 5) 
Periphlebitis retinae, (Clinical Volume 2, Chapter 5) (Clinical Volume 3, Chapter 16) See also Eales’ disease
Perkins tonometer, (Clinical Volume 3, Chapter 47) 
Pernicious anemia, ocular complications, (Clinical Volume 5, Chapter 23) 
Peroxidase-antiperoxidase techniques, in viral infection diagnosis, (Foundations Volume 2, Chapter 88) 
Peroxisomal disorders, (Clinical Volume 5, Chapter 31) 
cataracts associated with, (Clinical Volume 5, Chapter 41) 
Perphenazine, ocular toxicity, (Clinical Volume 5, Chapter 37) 
Persistence of fetal vasculature, (Foundations Volume 1, Chapter 40) 
Persistent fetal vasculature, angle-closure glaucoma and, 11, 12
Persistent hyperplastic primary vitreous, (Clinical Volume 3, Chapter 55) 
Persistent hyperplastic primary vitreous (PHPV). See Vitreous, primary, persistent hyperplasia
Personal protective equipment (PPE), occupational ophthalmology and, (Clinical Volume 5, Chapter 47) 
Perspex CQ. See Polymethylmethacrylate (PMMA)
Pervasive developmental disorders, (Clinical Volume 5, Chapter 42) 
Pethidine, vortex keratopathy and, (Clinical Volume 4, Chapter 17) 
Petrous bone, fractures, (Clinical Volume 2, Chapter 18) 
PET scanning. See Positron emission tomography
Peyman
full-thickness eye wall resection of, (Clinical Volume 4, Chapter 36) 
internal retinochoroidectomy of, (Clinical Volume 4, Chapter 36) 
iridocyclochoroidectomy of, (Clinical Volume 4, Chapter 36) 
Pfeiffer syndrome, (Foundations Volume 1, Chapter 41) (Clinical Volume 6, Chapter 110) See also Craniofacial anomalies, 10–11; (Foundations Volume 3, Chapter 17) 
PGI2. See Prostacyclin
PH
of blood, intraocular pressure and, (Foundations Volume 2, Chapter 7) 
of drugs
topical, bioinequivalence and, (Foundations Volume 3, Chapter 22) 
regulation of, in lens, (Clinical Volume 1, Chapter 72A) 
Phacoanaphylaxis, (Clinical Volume 3, Chapter 55) 
Phacoantigenic uveitis, (Clinical Volume 4, Chapter 55) See also Lens–induced uveitis
Phacodonesis, in exfoliation syndrome, (Clinical Volume 3, Chapter 54B) 
Phacoemulsification, (Clinical Volume 6, Chapter 3) (Clinical Volume 6, Chapter 56) (Clinical Volume 6, Chapter 6) (Clinical Volume 6, Chapter 6) 
bimanual ultrasound, (Clinical Volume 6, Chapter 7) 
bowl-out techniques, (Clinical Volume 6, Chapter 6) 
capsule polishing, (Clinical Volume 6, Chapter 6) 
chip and flip technique, (Clinical Volume 6, Chapter 7) 
choo-choo chop and flip technique, (Clinical Volume 6, Chapter 7) 
"chop" techniques, (Clinical Volume 6, Chapter 6) 
choroidal obstruction after, (Clinical Volume 3, Chapter 14) 
continuous curvilinear capsulorrhexis in, (Clinical Volume 6, Chapter 7) 
crack and flip technique, (Clinical Volume 6, Chapter 7) 
crater divide and conquer technique, (Clinical Volume 6, Chapter 7) 
divide techniques, (Clinical Volume 6, Chapter 6) 
glaucoma filtration surgery combined with, (Clinical Volume 6, Chapter 16) 
hydrodissection and hydrodelineation in, (Clinical Volume 6, Chapter 7) 
nucleofractis techniques, (Clinical Volume 6, Chapter 7) 
phaco chop technique, (Clinical Volume 6, Chapter 7) 
phaco fracture technique, (Clinical Volume 6, Chapter 7) 
power modulation, (Clinical Volume 6, Chapter 6) 
slow-motion phacoemulsification, (Clinical Volume 6, Chapter 6) 
suprascapular phacoemulsification, (Clinical Volume 6, Chapter 6) 
topical anesthesia, (Clinical Volume 6, Chapter 1) 
viscoelastic materials in, (Clinical Volume 6, Chapter 9) 
wound construction and architecture, (Clinical Volume 6, Chapter 7) 
Phacofragmentation. See Phacoemulsification
Phacogenic glaucoma, (Foundations Volume 3, Chapter 19) 
Phacogenic nongranulomatous uveitis, (Clinical Volume 4, Chapter 41) 
Phacolytic glaucoma. See Glaucoma, phacolytic
Phacomatoses, (Foundations Volume 3, Chapter 58) 
ocular manifestations, (Foundations Volume 3, Chapter 58) 
von Recklinghausen’s disease, (Foundations Volume 3, Chapter 58) 
Phacomorphic glaucoma. See Glaucoma, phacomorphic
Phagocytes, mononuclear, (Foundations Volume 2, Chapter 25) 
Phagocytosis, (Foundations Volume 3, Chapter 1) See also Macrophage(s)
photoreceptor outer segment, (Foundations Volume 1, Chapter 21) 
trabecular cells and, (Foundations Volume 1, Chapter 10) 
Phagolytic glaucoma, (Clinical Volume 3, Chapter 55) 
Phagosomes, in retinal pigment epithelium, (Clinical Volume 3, Chapter 1) 
Phakic intraocular lenses, (Clinical Volume 6, Chapter 11) 
angle-fixated phakic intraocular lenses, (Clinical Volume 6, Chapter 11) 
Alcon Anterior Chamber Phakic Intraocular Lens, (Clinical Volume 6, Chapter 11) 
iris-fixated phakic intraocular lenses, (Clinical Volume 6, Chapter 11) 
Artisan/Verisyse, (Clinical Volume 6, Chapter 11) 
Food and Drug Administration clinical study, (Clinical Volume 6, Chapter 11) 
posterior chamber phakic intraocular lenses, (Clinical Volume 6, Chapter 11) 
Medennium Phakic refractive lens, (Clinical Volume 6, Chapter 11) 
Phakomatoses, (Clinical Volume 2, Chapter 5) (Clinical Volume 2, Chapter 17) (Clinical Volume 3, Chapter 34)  (Clinical Volume 5, Chapter 36) See also specific disease; (Foundations Volume 3, Chapter 2) (Foundations Volume 3, Chapter 58)  (Clinical Volume 5, Chapter 36) 
angiomatosis
Sturge-Weber syndrome, (Foundations Volume 3, Chapter 58) 
von Hippel-Lindau disease, (Foundations Volume 3, Chapter 58) 
arteriovenous communication of retina and brain, (Foundations Volume 3, Chapter 2) 
Bourneville’s disease, (Clinical Volume 3, Chapter 34) 
Klippel Trenaunay-Weber syndrome, (Clinical Volume 5, Chapter 36) 
neurofibromatoses, (Clinical Volume 5, Chapter 36) 
retinal-neuro-cutaneous cavernous hemangioma syndrome, (Clinical Volume 3, Chapter 34) 
tuberous sclerosis complex, (Clinical Volume 5, Chapter 36) 
astrocytic retinal hamartomas, (Clinical Volume 5, Chapter 36) 
cutaneous findings, (Clinical Volume 5, Chapter 36) 
diagnostic criteria, (Clinical Volume 5, Chapter 36) 
intracranial lesions, (Clinical Volume 5, Chapter 36) 
mental retardation, (Clinical Volume 5, Chapter 36) 
neurologic findings, (Clinical Volume 5, Chapter 36) 
nonretinal features, (Clinical Volume 5, Chapter 36) 
ophthalmic features, (Clinical Volume 5, Chapter 36) 
pigmentary abnormalities, (Clinical Volume 5, Chapter 36) 
systemic features, (Clinical Volume 5, Chapter 36) 
visceral findings, (Clinical Volume 5, Chapter 36) 
type 2 neurofibromatosis, (Clinical Volume 5, Chapter 36) 
cutaneous findings, (Clinical Volume 5, Chapter 36) 
diagnostic criteria, (Clinical Volume 5, Chapter 36) 
neurologic findings, (Clinical Volume 5, Chapter 36) 
ophthalmic features, (Clinical Volume 5, Chapter 36) 
systemic features, (Clinical Volume 5, Chapter 36) 
visceral findings, (Clinical Volume 5, Chapter 36) 
Weskamp-Cotlier syndrome, (Clinical Volume 3, Chapter 34) 
Phakomatous choristoma, (Foundations Volume 3, Chapter 7) 
Pharmaceuticals, cataract from, (Clinical Volume 1, Chapter 73) 
Pharmacokinetics, (Foundations Volume 3, Chapter 23 ) 
of antibacterial agents, (Foundations Volume 2, Chapter 61) 
of antibiotics, postoperative prophylaxis and, (Foundations Volume 2, Chapter 64) 
of periocular injections, (Foundations Volume 3, Chapter 23 ) 
systemic therapy and, (Foundations Volume 3, Chapter 23 ) 
of topical medications, (Foundations Volume 3, Chapter 23 ) 
Pharmacologic agent effects on aqueous humor, (Foundations Volume 3, Chapter 25) 
intraocular pressure
non-steady-state alteration, by pharmacologic agents, (Foundations Volume 3, Chapter 25) 
non-steady-state alterations of, (Foundations Volume 3, Chapter 25) 
alpha-adrenergic agonists, (Foundations Volume 3, Chapter 25) 
beta-adrenergic agonists, (Foundations Volume 3, Chapter 25) 
beta-adrenergic antagonists, (Foundations Volume 3, Chapter 25) 
carbonic anhydrase inhibitors, (Foundations Volume 3, Chapter 25) 
cholinergic agents, (Foundations Volume 3, Chapter 25) 
prostaglandin analogues, (Foundations Volume 3, Chapter 25) 
steady-state alterations of, (Foundations Volume 3, Chapter 25) 
active and passive mechanisms of formation, (Foundations Volume 3, Chapter 25) 
alternative model for aqueous humor dynamics, (Foundations Volume 3, Chapter 25) 
aqueous humor formation, (Foundations Volume 3, Chapter 25) 
aqueous humor outflow, (Foundations Volume 3, Chapter 25) 
episcleral venous pressure, (Foundations Volume 3, Chapter 25) 
measurement of rate of aqueous humor formation, (Foundations Volume 3, Chapter 25) 
trabecular meshwork outflow, (Foundations Volume 3, Chapter 25) 
uveoscleral outflow, (Foundations Volume 3, Chapter 25) 
Pharmacologic paresis, (Foundations Volume 2, Chapter 9) 
Pharmacologic vitreolysis, (Foundations Volume 1, Chapter 16) (Foundations Volume 2, Chapter 11) 
prophylactic posterior vitreous detachment, (Foundations Volume 1, Chapter 16) 
replacing vitrectomy, (Foundations Volume 1, Chapter 16) 
vitreoretinal surgery adjuncts, (Foundations Volume 1, Chapter 16) 
Pharmacology. See also Drugs
of antibacterial agents, (Foundations Volume 2, Chapter 61) 
of antifungal drugs, (Foundations Volume 2, Chapter 62 ) 
of antiviral agents, (Foundations Volume 2, Chapter 100) 
of ocular beta-adrenergic antagonists, (Foundations Volume 3, Chapter 32 ) 
Phenacaine, ocular toxicity, (Clinical Volume 5, Chapter 37) 
Phenacetin, ocular toxicity, (Clinical Volume 5, Chapter 37) 
Phencyclidine, ocular toxicity, (Clinical Volume 5, Chapter 37) 
Phenelzine
Phenergan. See Promethazine
Phenmetrazine, ocular toxicity, (Clinical Volume 5, Chapter 37) 
Phenobarbital, ocular toxicity, (Clinical Volume 5, Chapter 37) 
Phenocopy, defined, (Foundations Volume 3, Chapter 51) 
Phenol red thread test, (Foundations Volume 2, Chapter 3) 
Phenothiazine derivatives, cataracts from, (Clinical Volume 5, Chapter 41) 
Phenothiazines
ocular teratogenicity, (Clinical Volume 5, Chapter 39) 
toxic retinopathies and, (Clinical Volume 3, Chapter 33) 
Phenothiazines, cataract with, (Clinical Volume 5, Chapter 41) 
Phenotype, defined, (Foundations Volume 3, Chapter 51) 
Phenoxybenzamine
effect on catecholamine systems, (Foundations Volume 3, Chapter 29) 
Phentermine, ocular toxicity, (Clinical Volume 5, Chapter 37) 
Phentolamine, effect on catecholamine systems, (Foundations Volume 3, Chapter 29) 
Phenylacetic acids. See Nonsteroidal anti-inflammatory drugs (NSAIDs)
Phenylalanine, oxidation, metabolic blocks, (Clinical Volume 4, Chapter 15) 
Phenylalkanoic acids. See Nonsteroidal anti-inflammatory drugs (NSAIDs)
Phenylbutazone, ocular toxicity, (Clinical Volume 5, Chapter 37) See Nonsteroidal anti–inflammatory drugs (NSAIDs)
Phenylephrine (Neo-synephrine), (Foundations Volume 3, Chapter 29) 
effect on aqueous humor, (Foundations Volume 3, Chapter 29) 
effect on catecholamine systems, (Foundations Volume 3, Chapter 29) 
effect on ciliary body, (Foundations Volume 3, Chapter 29) 
effect on conjunctiva, (Foundations Volume 3, Chapter 29) 
in glaucoma, malignant, (Clinical Volume 3, Chapter 53) 
ocular teratogenicity, (Foundations Volume 1, Chapter 39) 
pediatric dosage and administration of, (Clinical Volume 6, Chapter 81) 
systemic toxicity, (Clinical Volume 5, Chapter 37) 
in test for oculosympathetic paresis, (Clinical Volume 2, Chapter 15) 
Phenylketonuria, cataract in, (Clinical Volume 5, Chapter 41) 
Phenylpropanolamine, ocular toxicity, (Clinical Volume 5, Chapter 37) 
Phenytoin
and glaucoma incidence, (Clinical Volume 3, Chapter 57) 
neuroprotection of axons and, (Clinical Volume 3, Chapter 57) 
Phenytoin sodium (Dilantin)
Pheochromocytoma, (Clinical Volume 5, Chapter 21) 
in von Hippel-Lindau disease, (Clinical Volume 5, Chapter 36) 
Phlebitis, retinal. See also Retinal vasculitis
fluorescein angiography, (Clinical Volume 4, Chapter 57) 
Phlyctenular conjunctivitis, (Foundations Volume 3, Chapter 8) 
Phlyctenular keratoconjunctivitis, (Clinical Volume 4, Chapter 2) (Clinical Volume 4, Chapter 8)  (Clinical Volume 4, Chapter 8) 
causative agents, (Clinical Volume 4, Chapter 8) 
clinical manifestations, (Clinical Volume 4, Chapter 8) 
conjunctival phylctenulosis, (Clinical Volume 4, Chapter 8) 
corneal phylctenulosis, (Clinical Volume 4, Chapter 8) 
differential diagnosis, (Clinical Volume 4, Chapter 8) 
pathophysiologic considerations, (Clinical Volume 4, Chapter 8) 
symptoms, (Clinical Volume 4, Chapter 8) 
conjunctival phylctenulosis, (Clinical Volume 4, Chapter 8) 
corneal phylctenulosis, (Clinical Volume 4, Chapter 8) 
treatment, (Clinical Volume 4, Chapter 8) 
conjunctival phylctenulosis, (Clinical Volume 4, Chapter 8) 
nontuberculous phylctenulosis, (Clinical Volume 4, Chapter 8) 
tuberculous phylctenulosis, (Clinical Volume 4, Chapter 8) 
corneal phylctenulosis, (Clinical Volume 4, Chapter 8) 
PHMB (polyhexamethyl biguanide). See Polyhexanide
Phonologic dyslexia, (Clinical Volume 2, Chapter 7) 
Phoria
vertical, induced with bifocals, correction
compensated segments in, (Clinical Volume 1, Chapter 44) 
prism segments in, (Clinical Volume 1, Chapter 44) 
slab-off grinding in, (Clinical Volume 1, Chapter 44) 
Phosphocreatine deficiency, and retinal degeneration, in gyrate atrophy, (Clinical Volume 3, Chapter 25) 
Phospholine Iodide. See also Echothiophate iodide (Phospholine Iodide)
topical, (Clinical Volume 3, Chapter 56) See Echothiophate
Phospholipids, in rod disc membranes, (Foundations Volume 2, Chapter 12) 
Photapeutic keratectomy, (Clinical Volume 6, Chapter 47) 
excimer laser
therapeutic applications of, (Clinical Volume 6, Chapter 47) 
irregular surface, (Clinical Volume 6, Chapter 47) 
laser cornea interaction, (Clinical Volume 6, Chapter 47) 
lasik complications, (Clinical Volume 6, Chapter 47) 
photobiology of excimer laser corneal ablation, (Clinical Volume 6, Chapter 47) 
recurrent corneal erosions, (Clinical Volume 6, Chapter 47) 
superficial corneal opacities, (Clinical Volume 6, Chapter 47) 
topography-based ablations, (Clinical Volume 6, Chapter 47) 
Photic maculopathy, fluorescein angiography, (Foundations Volume 2, Chapter 113F) 
Photoablation. See also Ablation
Photobiology of excimer laser corneal ablation, (Clinical Volume 6, Chapter 47) 
Photobleaching, rhodopsin, (Foundations Volume 2, Chapter 12) 
Photochemistry, retinal, (Foundations Volume 2, Chapter 12) 
Photocoagulation
for age-related macular degeneration, (Clinical Volume 6, Chapter 76) 
angioid streaks and, (Clinical Volume 3, Chapter 36) 
in arterial macroaneurysm, (Clinical Volume 6, Chapter 76) 
in capillary hemangioma, (Clinical Volume 6, Chapter 76) 
for central serous chorioretinopathy, (Clinical Volume 6, Chapter 76) 
in chorioretinal diseases, (Clinical Volume 6, Chapter 76) 
choroidal neovascularization and, (Clinical Volume 6, Chapter 76) 
in Coats’ disease, (Clinical Volume 6, Chapter 76) 
for degenerative retinoschisis, (Clinical Volume 6, Chapter 76) 
delivery systems, (Clinical Volume 6, Chapter 76) 
in Eales’ disease, (Clinical Volume 3, Chapter 16) 
histopathologic effects, (Clinical Volume 6, Chapter 76) 
in histoplasmosis, (Clinical Volume 4, Chapter 48) 
instrument settings for, (Clinical Volume 6, Chapter 76) 
laser, (Clinical Volume 1, Chapter 69A)  (Clinical Volume 1, Chapter 69B ) 
in acute retinal necrosis syndrome, (Clinical Volume 3, Chapter 28) 
cyclophotocoagulation, (Clinical Volume 6, Chapter 19) 
in developmental glaucoma, (Clinical Volume 3, Chapter 51) 
in open-angle glaucoma, (Clinical Volume 3, Chapter 52) 
factors influencing, (Clinical Volume 1, Chapter 69A) 
goniophotocoagulation, (Clinical Volume 6, Chapter 19) 
indocyanine green angiography and, (Clinical Volume 3, Chapter 4A) 
light absorption by ocular pigments and, (Clinical Volume 1, Chapter 69A) 
light scattering and media absorption and, (Clinical Volume 1, Chapter 69A) 
for macular holes, (Clinical Volume 6, Chapter 61) 
power, spot size and exposure, (Clinical Volume 1, Chapter 69A) 
for retinal breaks, (Clinical Volume 6, Chapter 56) 
in sickle cell retinopathy, (Clinical Volume 3, Chapter 17 ) 
in macular edema, (Clinical Volume 6, Chapter 76) 
diabetes mellitus and, (Clinical Volume 5, Chapter 20) 
Nd: YAG laser, mechanism of, (Clinical Volume 6, Chapter 10) 
in pars planitis, (Clinical Volume 4, Chapter 43) 
for pathologic myopia, (Clinical Volume 3, Chapter 36) 
in periphlebitis retinae, (Clinical Volume 3, Chapter 16) 
in proliferative diabetic retinopathy, (Clinical Volume 6, Chapter 76) 
in radiation retinopathy, (Clinical Volume 3, Chapter 36A) 
in retinal degenerations, (Clinical Volume 6, Chapter 76) 
in retinal detachment, subclinical, (Clinical Volume 6, Chapter 76) 
in retinal vascular diseases, (Clinical Volume 6, Chapter 76 ) 
in retinoblastoma, (Clinical Volume 6, Chapter 109) 
in retinopathy of prematurity (retrolental fibroplasia), (Clinical Volume 6, Chapter 76) 
in retinoschisis, juvenile, (Clinical Volume 3, Chapter 9) 
in sickle thalassemia, (Clinical Volume 6, Chapter 76) 
in subretinal neovascular membranes, (Clinical Volume 6, Chapter 76) 
in toxoplasmosis, (Clinical Volume 4, Chapter 46) 
Photocoagulation of ciliary processes, (Clinical Volume 1, Chapter 69B) 
Photodisruption, lasers and, in keratomileusis, (Clinical Volume 6, Chapter 46) 
Photodynamic therapy, (Clinical Volume 1, Chapter 69C Chapter(6)63) (Foundations Volume 2, Chapter 110A) 
for angioid streaks, (Clinical Volume 3, Chapter 36) 
clinical mechanism, (Clinical Volume 6, Chapter 63) 
cost-effectiveness, (Clinical Volume 6, Chapter 63) 
experimental mechanism, (Clinical Volume 6, Chapter 63) 
in histoplasmosis, (Clinical Volume 4, Chapter 48) 
historical perspective, (Clinical Volume 1, Chapter 69C) 
light terminology, (Clinical Volume 1, Chapter 69C) 
for pathologic myopia, (Clinical Volume 3, Chapter 36) 
physiologic basis, (Clinical Volume 1, Chapter 69C) 
quality-of-life after, (Clinical Volume 6, Chapter 63) 
in subfoveal choroidal neovascularization, (Clinical Volume 6, Chapter 63) 
Photoelectric oculography, (Clinical Volume 2, Chapter 9) 
Photofrin, photodynamic therapy, (Clinical Volume 1, Chapter 69C) 
Photographic documentation, of ultrasound examination, (Foundations Volume 2, Chapter 108) 
Photography
of eye movements, (Clinical Volume 2, Chapter 9) 
fundus. (See Fundus, photography; Fundus cameraof)
Scheimpflug, densitometry of photographs, (Clinical Volume 1, Chapter 31) 
slit lamp, in cataract, Scheimpflug cameras, (Clinical Volume 1, Chapter 31) 
Photokeratoscope, (Clinical Volume 1, Chapter 33) (Clinical Volume 1, Chapter 65) See also Keratoscope; Keratoscopy; Videokeratoscope; Videokeratoscopy
Photophobia
in monochromatism, rod, (Clinical Volume 3, Chapter 9) 
in progressive cone-rod dystrophies, (Clinical Volume 3, Chapter 9) 
Photopic stress test, in ocular ischemic syndrome, (Clinical Volume 3, Chapter 12) (Foundations Volume 2, Chapter 13) 
Photopic vision, cones, (Clinical Volume 1, Chapter 33) 
Photopigments. See Pigment(s)
Photoreceptor(s), retinal, 2–6. See also Cones; Rods; (Clinical Volume 2, Chapter 2) (Clinical Volume 2, Chapter 4) (Clinical Volume 3, Chapter 1) (Foundations Volume 2, Chapter 13) 
age-related changes, (Foundations Volume 1, Chapter 19) 
basal body (centriole), (Clinical Volume 3, Chapter 1) 
chemistry of outer segments of, (Foundations Volume 2, Chapter 12) 
in chromatic aberration, (Clinical Volume 1, Chapter 33) 
classes, in primate, (Foundations Volume 1, Chapter 20) 
cone degenerations, macular, (Clinical Volume 2, Chapter 5) 
cone dystrophies, (Clinical Volume 3, Chapter 9) 
connecting cilia, (Clinical Volume 3, Chapter 1) 
contribution to pupillary light reflex, (Foundations Volume 2, Chapter 9) 
“dark current, ”, (2) 13: 3
database entries containing term, (Foundations Volume 1, Chapter 19A) 
degeneration
progressive. (See Retinitis pigmentosa)
density from nasal to temporal edge of retina, (Clinical Volume 1, Chapter 33) 
differentiation, retinoblastoma and, (Foundations Volume 3, Chapter 21) 
directional sensitivity of, (Foundations Volume 2, Chapter 20) 
distribution across retina, 2, (Foundations Volume 2, Chapter 14) 
external limiting membrane of, (Foundations Volume 1, Chapter 19) 
immunocytochemistry, (Clinical Volume 3, Chapter 1) 
inner plexiform layer of, (Foundations Volume 1, Chapter 19) 
neural connections, (Clinical Volume 1, Chapter 33) 
outer nuclear layer of, (Foundations Volume 1, Chapter 19) 
outer plexiform layer. (See Outer plexiform layer (OPL))
outer plexiform layer of, (Foundations Volume 1, Chapter 19) 
in photopic vision, (Clinical Volume 1, Chapter 33) 
photoresponse model, (Clinical Volume 3, Chapter 2) 
resolution of diffracted images and, (Clinical Volume 1, Chapter 33) 
scotopic vision, (1)33: 25in
triads, (3)1: 9, 10
visual pigments, (Clinical Volume 3, Chapter 1) 
Photorefractive keratectomy, (Clinical Volume 6, Chapter 48) 
Photorefractive keratectomy (PRK), (Clinical Volume 1, Chapter 64) 
Photorefractive keratoplasty, myopia correction and, (Clinical Volume 1, Chapter 42) 
Photosensitizers, photodynamic therapy, (Clinical Volume 1, Chapter 69C) 
Photostress, in diabetic retinopathy, (Clinical Volume 3, Chapter 30) 
Photostress test, (Clinical Volume 2, Chapter 2) 
Photostress test, neuro-ophthalmologic examination, (Clinical Volume 2, Chapter 10) 
Phototherapy, for neonatal jaundice, (Clinical Volume 5, Chapter 39) 
Phototoxicity. See also Light toxicity
Phototransduction, (Foundations Volume 2, Chapter 12) 
cascade, adaptation and, (Foundations Volume 2, Chapter 16) 
PHPV (persistent hyperplastic primary vitreous). See See Vitreous, persistent hyperplastic primary; Vitreous, primary, persistent hyperplasia
Phthirus pubis, of lids, (Clinical Volume 4, Chapter 22) 
Phycomycosis. See Mucormycosis (phycomycosis)
Phylctenulosis
Phylogenetics, of binocular vision, (Foundations Volume 2, Chapter 24) 
Physical optics, (Clinical Volume 1, Chapter 31) See also Geometric optics; Light
antireflection coatings, (Clinical Volume 1, Chapter 31) 
Aristotle’s ether theory, (Clinical Volume 1, Chapter 31) 
atomic structure, (Clinical Volume 1, Chapter 31) 
diffraction effects, (Clinical Volume 1, Chapter 31) 
Fresnel’s ether theory, (Clinical Volume 1, Chapter 31) 
Huygen’s theory of light, (Clinical Volume 1, Chapter 31) 
laser interferometry, (Clinical Volume 1, Chapter 31) 
Maxwell’s equations, (Clinical Volume 1, Chapter 31) 
Newton’s theory of light, (Clinical Volume 1, Chapter 31) 
optical coherence tomography, (Clinical Volume 1, Chapter 31) 
Planck’s constant, (Clinical Volume 1, Chapter 31) 
polarization phenomena, (Clinical Volume 1, Chapter 31) 
Haidinger brushes, (Clinical Volume 1, Chapter 31) 
Scheimpflug principle, (Clinical Volume 1, Chapter 31) 
Physiologic diplopia, (Clinical Volume 1, Chapter 5) 
Physiologic myopia, (Clinical Volume 3, Chapter 36) 
Physiologic nystagmus, (Clinical Volume 2, Chapter 11) 
Physostigmine
for atropine toxicity, (Clinical Volume 1, Chapter 41) 
systemic toxicity, (Clinical Volume 5, Chapter 37) 
Physostigmine (Eserine), side effects of, in infants and children, (Foundations Volume 3, Chapter 43) 
Physostigmine salicylate (Antilirium), as antidote for anticholinergic toxicity, (Foundations Volume 3, Chapter 43) 
Phytanic acid storage disease. See Refsum’s disease
Phytohemagglutinin, (Foundations Volume 2, Chapter 35) 
Pial arterial plexus, (Clinical Volume 2, Chapter 4) 
Pickford-Nicolson anomaloscope, (Foundations Volume 2, Chapter 19) 
Piggy-back lenses, (Clinical Volume 1, Chapter 56) 
Pigmentary changes, trauma to iris and, (Clinical Volume 4, Chapter 61) 
Pigmentary dystrophy
butterfly-shaped, molecular genetics, (Foundations Volume 3, Chapter 55) 
Pigmentary glaucoma, (Foundations Volume 3, Chapter 19) 
trabecular meshwork in, (Foundations Volume 1, Chapter 10) 
Pigmentary retinopathies. See Retinopathy, pigmentary
Pigmentary retinopathy in systemic mucopolysaccaridoses, (Clinical Volume 5, Chapter 30) 
Pigmentation
albinism, (Clinical Volume 4, Chapter 38) See also Albinismin
in angioid streaks, (Clinical Volume 4, Chapter 66) 
in Chediak-Higashi syndrome, (Clinical Volume 5, Chapter 27) 
in choroideremia, (Clinical Volume 4, Chapter 66) 
in incontinentia pigmenti, (Clinical Volume 5, Chapter 27) 
lenticular, congenital, (Foundations Volume 1, Chapter 15) 
of macula lutea, and chromatic blur, (Clinical Volume 1, Chapter 33) 
in xeroderma pigmentosum, (Clinical Volume 5, Chapter 27) 
Pigment epithelial detachments, (Clinical Volume 3, Chapter 36) 
Pigment epithelial dystrophy of Noble-Carr-Siegal, (Clinical Volume 3, Chapter 9) 
Pigment epithelium, (Foundations Volume 1, Chapter 11) 
Pigment epithelium, retinal. See Retinal pigment epithelium
Pigment pattern dystrophies, (Foundations Volume 3, Chapter 60) 
fluorescein angiography, (Foundations Volume 2, Chapter 113B) 
Pigment release, muscarinic antagonists and, (Foundations Volume 3, Chapter 26) 
Pigment(s). See also specific pigments
corneal deposition, (Foundations Volume 3, Chapter 9) 
in diabetes mellitus, (Foundations Volume 3, Chapter 18) 
molecular biology of, (Foundations Volume 2, Chapter 19) 
Pilar (trichilemmal) cysts, (Foundations Volume 3, Chapter 7) 
Pili
gram-negative bacilli, (Foundations Volume 2, Chapter 52) 
Pilocar. See Pilocarpine
Pilocel. See Pilocarpine
Pilocytes, in optic nerve gliomas, (Clinical Volume 2, Chapter 42) 
Pilopine HS Gel, topical, (Clinical Volume 3, Chapter 56) 
Pimaricin. See Natamycin
Pincushion distortion, (Clinical Volume 1, Chapter 30) 
Pindolol, pharmacology of, (Foundations Volume 3, Chapter 32) 
Pingueculae, conjunctival, (Clinical Volume 4, Chapter 16) 
phlyctenular keratoconjunctivitis versus, (Clinical Volume 4, Chapter 8) 
ultraviolet radiation and, (Clinical Volume 5, Chapter 55) 
Pinocytosis, blood-aqueous humor barrier and, (Foundations Volume 3, Chapter 23) 
Pinocytotic vesicles, (Foundations Volume 2, Chapter 5) 
Pinpoint luminosities, (Clinical Volume 2, Chapter 1) 
Piperazine, ocular toxicity, (Clinical Volume 5, Chapter 37) 
Piperocaine, ocular toxicity, (Clinical Volume 5, Chapter 37) 
Piroxicam. See Nonsteroidal anti-inflammatory drugs (NSAIDs)
Pits
optic nerve, (Foundations Volume 3, Chapter 16) 
serous macular detachment secondary to, optical coherence tomography, (Foundations Volume 2, Chapter 107) 
Pituitary adenoma, (Clinical Volume 5, Chapter 32) 
Pituitary apoplexy, (Clinical Volume 2, Chapter 6) 
chiasmal syndromes in, (Clinical Volume 2, Chapter 6) 
Pityriasis versicolor, (Foundations Volume 2, Chapter 54) 
Pityrosporum orbiculare, (Foundations Volume 3, Chapter 7) 
Pityrosporum orbiculare, and seborrheic blepharitis, (Clinical Volume 4, Chapter 22) 
Pityrosporum ovale, and seborrheic blepharitis, (Clinical Volume 4, Chapter 22) 
Pityrosporum ovale (orbiculare), (Foundations Volume 3, Chapter 7) 
Pizotifen, for migraine, (Clinical Volume 2, Chapter 16) 
“Pizza-pie” pattern, in cytomegalovirus retinitis, (Clinical Volume 3, Chapter 7) (Clinical Volume 3, Chapter 28A) 
Placidyl. See Ethchlorvynol
Placoid chorioretinitis, syphilitic posterior, (Clinical Volume 4, Chapter 57) 
Plain roentgenogram evaluation of orbital disease. See Orbital disease, plain roentgenogram evaluation of
Planes of unit magnification, in ray sketching, (Clinical Volume 1, Chapter 30) 
Plaque keratopathy, (Clinical Volume 4, Chapter 17) 
Plaquenil retinopathy, EOG in, (Foundations Volume 2, Chapter 14) 
Plaques
anchoring, corneal, (Foundations Volume 1, Chapter 8) 
attachment, vitreous, (Foundations Volume 1, Chapter 16) 
episcleral, radiotherapy
in posterior uveal melanoma, (Clinical Volume 6, Chapter 70) 
fibrous, forehead, in tuberous sclerosis, (Clinical Volume 5, Chapter 36) 
scleral
hyaline, ultrasound biomicroscopy, (Foundations Volume 2, Chapter 106) 
Plasma cell tumors, (Clinical Volume 2, Chapter 39) See also Multiple myeloma
solitary, optic nerves, (Clinical Volume 2, Chapter 5) 
Plasma osmolality
aqueous formation and, (Foundations Volume 2, Chapter 6) 
intraocular pressure and, (Foundations Volume 2, Chapter 7) 
Plasmapheresis
effects on immune system, (Foundations Volume 2, Chapter 31) 
effects on ocular inflammatory disease, (Foundations Volume 2, Chapter 31) 
in ocular inflammation, (Foundations Volume 2, Chapter 31) 
Plasmin, in diabetic vitrectomy, (Clinical Volume 6, Chapter 57) 
pharmacologic vitreolysis, (Foundations Volume 2, Chapter 11) 
Plastic implants. See Implants
Plastic lenses, Fresnel membrane, (Clinical Volume 1, Chapter 52) 
Plastic surgery. See Reconstructive surgery
Platelet-activating factor (PAF), in inflammation, (Foundations Volume 2, Chapter 27) 
Platelet aggregation, inhibitors. See Antiplatelet agents
Platelet-derived growth factor, and lens of eye, (Clinical Volume 1, Chapter 72A) 
Platelet disorders and coagulopathies, (Clinical Volume 3, Chapter 18) 
Platelet-fibrin emboli, in carotid artery disease, (Clinical Volume 3, Chapter 14) 
Platybasia. See Basilar impressions of skull
Pleiotropism, defined, (Foundations Volume 3, Chapter 51) 
Pleomorphic adenocarcinoma, (Clinical Volume 2, Chapter 40) 
Pleomorphic adenoma, (Foundations Volume 3, Chapter 17) See Adenoma, pleomorphic
Pleomorphic rhabdomyosarcoma. See Rhabdomyosarcoma
Pleomorphism, corneal endothelial, contact lens-associated, (Clinical Volume 4, Chapter 27) 
Pleoptics, in amblyopia, (Clinical Volume 1, Chapter 11) 
Plica lacrimalis. See Valve of Hasner
Plica semilunaris, caruncle, (Foundations Volume 2, Chapter 2) 
PMNs. See Leukocytes, polymorphonuclear
PMR. See Polymyalgia rheumatica
Pneumatic displacement, (Clinical Volume 6, Chapter 68) 
Pneumatic tonometer, (Foundations Volume 2, Chapter 7) 
Pneumatization, paranasal sinus, (Foundations Volume 1, Chapter 32) 
Pneumatoceles, lacrimal sac, (Foundations Volume 1, Chapter 32) 
Pneumococcal infection, conjunctivitis, (Foundations Volume 2, Chapter 49) 
Pneumococci, conjunctivitis from, (Clinical Volume 4, Chapter 8) 
Pneumocystis carinii pneumonia, in AIDS, choroiditis and, (Clinical Volume 4, Chapter 37) 
Pneumoplethysmography, in cranial arteritis, (Clinical Volume 2, Chapter 5) 
Pneumotonograph, (Clinical Volume 3, Chapter 47) 
ischemic optic neuropathy and, common versus arteritic, (Clinical Volume 2, Chapter 5) 
POHS. See Presumed ocular histoplasmosis syndrome
Poikiloderma congenitale. See Rothmund’s syndrome
Point-by-point comparisons, in field defect progression assessment, (Clinical Volume 3, Chapter 49) 
Point mutation detection, (Foundations Volume 1, Chapter 19A) 
Polarimetry, laser, in glaucoma, (Clinical Volume 3, Chapter 52) 
Polarization phenomena, (Clinical Volume 1, Chapter 31 ) 
bee polarization, (Clinical Volume 1, Chapter 31) 
corneal birefringence, (Clinical Volume 1, Chapter 31) 
Haidinger brushes, (Clinical Volume 1, Chapter 31) 
Polaroid, (Clinical Volume 1, Chapter 31) 
vectographs. (See Vectographic studies)
Poliosis, in staphylococcal lid infections, (Clinical Volume 4, Chapter 22) 
Polo, eye injuries from, protective device effectiveness and, (Clinical Volume 5, Chapter 45) 
Polyamine excess
and retinal degeneration
in gyrate atrophy, (Clinical Volume 3, Chapter 25) 
Polyaminopropylbiguanide, in contact lens care, (Foundations Volume 2, Chapter 80) 
Polydystrophic dwarfism. See Maroteaux-Lamy syndrome
Polydystrophic oligophrenia. See Sanfilippo syndrome
Polyene antifungal agents, (Foundations Volume 2, Chapter 62) See also Amphotericin B
Polygenic disorders, (Foundations Volume 3, Chapter 51) 
Polyhexamethyl biguanide (PHMB). See Polyhexanide
Polymegethism, corneal endothelial, contact lens-associated, (Clinical Volume 4, Chapter 27) 
Polymerase chain reaction, (Foundations Volume 2, Chapter 40B) 
anterior segment, external disease, (Foundations Volume 2, Chapter 40B) 
application to clinical problems, (Foundations Volume 2, Chapter 40B) 
delayed-onset postoperative endophthalmitis, (Foundations Volume 2, Chapter 40B) 
ocular toxoplasmosis, (Foundations Volume 2, Chapter 40B) 
traditional detection techniques, compared, (Foundations Volume 2, Chapter 40B) 
variants of, (Foundations Volume 2, Chapter 40B) 
multiplex polymerase chain reaction, (Foundations Volume 2, Chapter 40B) 
nested polymerase chain reaction, (Foundations Volume 2, Chapter 40B) 
real-time quantitative polymerase chain reaction, (Foundations Volume 2, Chapter 40B) 
reverse transcription-polymerase chain reaction, (Foundations Volume 2, Chapter 40B) 
universal primer polymerase chain reaction, (Foundations Volume 2, Chapter 40B) 
Polymethylmethacrylate (PMMA)
complications of lenses, (Clinical Volume 4, Chapter 27) See also Contact lenses, complications
corneal hypoesthesia and, (Clinical Volume 4, Chapter 27) 
Polymorphic macular degeneration of Braley, (Clinical Volume 3, Chapter 9) 
Polymorphic reticulosis, (Clinical Volume 2, Chapter 35) See also Lymphomatoid granulomatosis
Polymorphic stromal dystrophy, (Foundations Volume 3, Chapter 63) 
Polymorphic variations, DNA, (Foundations Volume 3, Chapter 51) 
Polymorphic vitelliform macular dystrophy. See Best’s vitelliform dystrophy
Polymorphism, restriction fragment length, (Foundations Volume 1, Chapter 19A) 
Polymorphonuclear leukocytes, inflammation and, (Foundations Volume 2, Chapter 42) 
Polymorphonuclear neutrophils, in chemical injuries, (Clinical Volume 4, Chapter 28) 
Polymyalgia rheumatica (PMR), (Clinical Volume 2, Chapter 5) 
Polymyxin B, (Clinical Volume 4, Chapter 26) (Foundations Volume 2, Chapter 61) 
for conjunctivitis and keratitis, (Foundations Volume 3, Chapter 39) 
in corneal ulcers, (Clinical Volume 4, Chapter 18) 
fortified topical preparations, (Clinical Volume 4, Chapter 18) 
side effects, in infants and children, (Foundations Volume 3, Chapter 43) 
subconjunctival dose, (Clinical Volume 4, Chapter 18) 
systemic toxicity, (Clinical Volume 5, Chapter 37) 
trimethoprim and. (See Trimethoprim/polymyxin B sulfate)
Polyneuritis
cranial, idiopathic, (Foundations Volume 1, Chapter 37) 
Polyneuropathy, cranial, (Clinical Volume 2, Chapter 12) (Foundations Volume 1, Chapter 36) 
acute infectious. (See also Guillain-Barre syndrome)
oculomotor palsy, (Clinical Volume 2, Chapter 12) 
Polypoidal choroidal neovascularization, (Foundations Volume 2, Chapter 110A) 
Polypoidal choroidal vasculopathy, idiopathic, (Clinical Volume 3, Chapter 4A) (Clinical Volume 3, Chapter 22) 
Polyposis coli, adenomatous, familial, (Clinical Volume 5, Chapter 30) 
Polyradiculopathy, (Clinical Volume 2, Chapter 8) 
Polysaccharide-iron complex, ocular toxicity, (Clinical Volume 5, Chapter 37) 
Polysulfone, in intrastromal lenses, (Clinical Volume 1, Chapter 64) 
Polytetrafluoroethylene (PTFE), in lid reconstruction, (Clinical Volume 5, Chapter 88) 
Polytrim. See Trimethoprim/polymyxin B sulfate
Polyvinyl alcohol, in ophthalmic solutions, and bioavailability, (Foundations Volume 3, Chapter 22) 
Pompe disease. See Glycogen storage disease
Pons, (Clinical Volume 2, Chapter 8) 
lesions of, horizontal gaze in, (Clinical Volume 2, Chapter 10) 
Pons, lesions of, effect on horizontal gaze, (Clinical Volume 2, Chapter 10) 
Pontine nuclei, ocular motility and, (Foundations Volume 2, Chapter 23) 
Popov glands, (Foundations Volume 1, Chapter 32) See also Lacrimal glands
Population sampling, in ophthalmic epidemiology, (Foundations Volume 2, Chapter 43) 
correlational studies, (Foundations Volume 2, Chapter 43) 
Porcine collagen lenses, (Clinical Volume 4, Chapter 11) 
Porfimer sodium (Photofrin), photodynamic therapy, (Clinical Volume 1, Chapter 69C) 
PORN. See Progressive outer retinal necrosis
Porocarcinoma, eccrine, (Foundations Volume 3, Chapter 7) 
Positional changes, effect on intraocular pressure, (Foundations Volume 2, Chapter 7) 
Positional cloning, (Foundations Volume 3, Chapter 55) 
Positional nystagmus, (Clinical Volume 2, Chapter 11) 
Position-vestibular-pause cells, (Foundations Volume 2, Chapter 23) 
Positive visual phenomena, (Clinical Volume 2, Chapter 7) 
visual hallucinations, (Clinical Volume 2, Chapter 7) 
with altered mental states, (Clinical Volume 2, Chapter 7) 
Charles Bonnet’s syndrome, (Clinical Volume 2, Chapter 7) 
with cognitive dysfunction, (Clinical Volume 2, Chapter 7) 
during eye closure, (Clinical Volume 2, Chapter 7) 
hallucinatory states, (Clinical Volume 2, Chapter 7) 
migrainous hallucinations, (Clinical Volume 2, Chapter 7) 
peduncular hallucinations, (Clinical Volume 2, Chapter 7) 
release hallucinations, (Clinical Volume 2, Chapter 7) 
visual seizures, (Clinical Volume 2, Chapter 7) 
visual perseveration, (Clinical Volume 2, Chapter 7) 
cerebral polyopia, (Clinical Volume 2, Chapter 7) 
Positron emission tomography, in visual cortex imaging, (Foundations Volume 1, Chapter 34) (Foundations Volume 2, Chapter 22) 
Positron emission tomography (PET), in amblyopia, (Clinical Volume 1, Chapter 10) 
Posner-Inglima tonometer, (Foundations Volume 2, Chapter 7) 
Posner-Schlossman syndrome, (Clinical Volume 3, Chapter 55) (Clinical Volume 4, Chapter 40) (Clinical Volume 4, Chapter 54) See also Glaucomatocyclitic crisis
Posner-Schlossman syndrome. See Glaucomatocyclitic crisis
Posterior apical radius (PAR), (Clinical Volume 1, Chapter 55) 
Posterior capsule
management, in cataract surgery, pediatric, (Clinical Volume 6, Chapter 100) 
Posterior capsulotomy
Posterior chamber
anatomy
Posterior chamber intraocular lens. See also Intraocular lenses
epikeratoplasty as alternative to, (Clinical Volume 6, Chapter 45) 
Posterior chamber intraocular lenses, (Clinical Volume 6, Chapter 8) 
Posterior chamber lenses, (Clinical Volume 6, Chapter 11) 
Posterior commissure
Collier’s sign, (Clinical Volume 2, Chapter 3) 
eye movements and, (Clinical Volume 1, Chapter 4) 
lesions affecting, (Clinical Volume 2, Chapter 10) 
Posterior corneal defect. See Peters’ anomaly
Posterior embryotoxon, (1)53: 15
Posterior hyaloid face, (Clinical Volume 6, Chapter 56) 
Posterior internuclear ophthalmoplegia of Lutz, (Clinical Volume 2, Chapter 10) 
Posterior lenticonus, (Clinical Volume 5, Chapter 41) 
Posterior polymorphous dystrophy
characteristics of, (Foundations Volume 1, Chapter 9) 
differential diagnosis, (Foundations Volume 3, Chapter 19) 
Posterior scleral foramen, (Foundations Volume 1, Chapter 1) 
Posterior segment injuries, (Clinical Volume 3, Chapter 31) 
choroidal injuries, (Clinical Volume 3, Chapter 31) 
commotio retinae, (Clinical Volume 3, Chapter 31) 
optic nerve injuries, (Clinical Volume 3, Chapter 31) 
retinal, vitreous hemorrhage, (Clinical Volume 3, Chapter 31) 
retinal detachment, (Clinical Volume 3, Chapter 31) 
retinal tears, (Clinical Volume 3, Chapter 31) 
role of head trauma in, (Clinical Volume 3, Chapter 31) 
vitreous traction tears, (Clinical Volume 3, Chapter 31) 
retinitis sclopeteria, (Clinical Volume 3, Chapter 31) 
Posterior segment of eye. See also specific structure
in sickle cell disease, (Clinical Volume 3, Chapter 17 ) 
Posterior segment opportunistic infections, (Clinical Volume 5, Chapter 40) 
Posterior subcapsular cataract, (Clinical Volume 1, Chapter 73) 
Posterior synechiae formation as complication of hyphema, (Clinical Volume 4, Chapter 61) 
Posterior uveal bleeding syndrome, (Clinical Volume 3, Chapter 22) 
Posterior uveal melanoma
counseling patient, (Clinical Volume 6, Chapter 70) 
orbital exenteration, (Clinical Volume 6, Chapter 70) 
periodic observation, (Clinical Volume 6, Chapter 70) 
photocoagulation, (Clinical Volume 6, Chapter 70) 
surgical management, (Clinical Volume 6, Chapter 70) 
systemic metastasis, management of, (Clinical Volume 6, Chapter 70) 
transpupillary thermapy, (Clinical Volume 6, Chapter 70) 
Posterior uveitis. See Uveitis, posterior
Posterior vermis, ocular motility and, (Foundations Volume 2, Chapter 23) 
Posterior vitreous cortex, (Foundations Volume 2, Chapter 11) 
Posterior vitreous detachment, (Foundations Volume 1, Chapter 16) 
Postgeniculate structures, visual loss arising from, (Clinical Volume 2, Chapter 1) 
Postherpetic neuralgia, (Foundations Volume 1, Chapter 36) 
Postjunctional receptors, (Foundations Volume 3, Chapter 26) 
Postsynaptic receptors, (Foundations Volume 1, Chapter 20) 
Posttraumatic injuries, specialty lenses after, (Clinical Volume 1, Chapter 56) 
Postures, compensatory, (Clinical Volume 1, Chapter 6) 
Posturography, vestibular system assessment, (Clinical Volume 2, Chapter 18) 
Potassium
carbonic anhydrase inhibitors and, (Foundations Volume 3, Chapter 30) 
Potassium iodide, in cataracts, (Clinical Volume 1, Chapter 71) 
Povidone-iodine
prophylaxis
endophthalmitis, (4)55: 7–8for
Power
optical. (See Optical power)
paraxial, of spherical surface, (Clinical Volume 1, Chapter 30) 
of prism, vector calculation of, (Clinical Volume 1, Chapter 30) 
Power cross, spherocylinder, (Clinical Volume 1, Chapter 30) 
Poxviruses
replication cycle of, (Foundations Volume 2, Chapter 97) 
PPD (purified protein derivative) test, in tuberculosis, (Clinical Volume 4, Chapter 58) 
PPE. See Personal protective equipment
PPRF. See Pontine paramedian reticular formation
Practolol
Prader-Willi syndrome, (Foundations Volume 3, Chapter 59) 
Pralidoxime (Protopam), as antidote for anticholinesterase poisoning, (Foundations Volume 3, Chapter 43) 
Prazosin, effect on catecholamine systems, (Foundations Volume 3, Chapter 29) 
Prebetalipoproteinemia, (Clinical Volume 4, Chapter 15) 
Prechiasmal pathways and disorders, (Clinical Volume 2, Chapter 5) 
Precipitates
inflammatory, on trabecular meshwork, (Clinical Volume 3, Chapter 54D) 
Precipitin procedures, (Foundations Volume 2, Chapter 40) 
Pre-Descemet dystrophy, (Foundations Volume 3, Chapter 63) 
Pre-Descemet membrane dystrophies, (Clinical Volume 4, Chapter 16) 
Prednisolone, (Foundations Volume 3, Chapter 31) 
in endophthalmitis, (Clinical Volume 4, Chapter 24) 
in infants and children, (Foundations Volume 3, Chapter 43) 
postoperative, after penetrating keratoplasty, (Clinical Volume 6, Chapter 26) 
Prednisone, (Foundations Volume 3, Chapter 31) See also Corticosteroids
in rickettsial disease, (Foundations Volume 2, Chapter 58) 
in temporal arteritis, (Foundations Volume 3, Chapter 31) 
Prednisone. See also Corticosteroid therapy
in arteritic ischemic optic neuropathy, (Clinical Volume 2, Chapter 5) 
for erythema multiforme, (Clinical Volume 4, Chapter 12) 
in hemangioma, capillary, (Clinical Volume 2, Chapter 37) 
in histoplasmosis, (Clinical Volume 4, Chapter 48) 
for orbital inflammation, (Clinical Volume 2, Chapter 35) 
for pemphigoid
for toxoplasmosis, (Clinical Volume 4, Chapter 46) 
toxoplasmosis recurrence with, (Clinical Volume 4, Chapter 46) 
in Wegener’s granulomatosis, (Clinical Volume 2, Chapter 35) 
Predominantly antibody defects, lymphocyte disorders and, (Clinical Volume 5, Chapter 40) 
Pre-eclampsia, eclampsia, (Clinical Volume 5, Chapter 32) 
choroidopathy in, (Clinical Volume 5, Chapter 32) 
cortical vision loss in, (Clinical Volume 5, Chapter 32) 
Pre-eclampsia and eclampsia, (Clinical Volume 5, Chapter 32) 
Preferential looking test, (Clinical Volume 5, Chapter 51) 
Preferential path, for incisions, (Clinical Volume 6, Chapter 3) 
Preferred numbers series, (Clinical Volume 5, Chapter 51) 
Prefrontal cortex
dorsolateral, ocular motility and, (Foundations Volume 2, Chapter 23) 
dorsomedial, ocular motility and, (Foundations Volume 2, Chapter 23) 
Pregnancy, (Clinical Volume 5, Chapter 32) 
after retinal detachment surgery, (Clinical Volume 5, Chapter 32) 
arteriovenous malformations, (Clinical Volume 2, Chapter 17) 
Bell’s palsy in, (Clinical Volume 2, Chapter 8) 
conditions arising during, (Clinical Volume 5, Chapter 32) 
contact lens tolerance in, (Clinical Volume 5, Chapter 32) 
diabetic retinopathy, (Clinical Volume 5, Chapter 32) 
diabetic retinopathy and, (Clinical Volume 6, Chapter 76) 
disorders related to, (Clinical Volume 5, Chapter 32) 
drug use during. (See Teratogenicity)
effects on mother’s eye, (Clinical Volume 5, Chapter 32 ) 
preexisting disorders and, (Clinical Volume 5, Chapter 32) 
ergot preparations in, (Clinical Volume 2, Chapter 16) 
field defects in, (Clinical Volume 2, Chapter 6) 
fluorescein angiography in, (Clinical Volume 5, Chapter 32) 
intracranial disorders in, (Clinical Volume 5, Chapter 32) 
amniotic fluid or air embolism, (Clinical Volume 5, Chapter 32) 
benign intracranial hypertension, (Clinical Volume 5, Chapter 32) 
carotid-cavernous fistulae, (Clinical Volume 5, Chapter 32) 
cerebral venous, sinus thrombosis, (Clinical Volume 5, Chapter 32) 
intracranial aneurysms, arteriovenous malformations, (Clinical Volume 5, Chapter 32) 
intracranial meningioma, (Clinical Volume 5, Chapter 32) 
lymphocytic hypophysitis, (Clinical Volume 5, Chapter 32) 
metastatic choriocarcinoma, (Clinical Volume 5, Chapter 32) 
pituitary adenoma, (Clinical Volume 5, Chapter 32) 
labor and delivery-related disorders, (Clinical Volume 5, Chapter 32) 
neuro-ophthalmologic changes, (Clinical Volume 5, Chapter 32) 
neuro-ophthalmologic changes in, (Clinical Volume 5, Chapter 32) 
normal pituitary, (Clinical Volume 5, Chapter 32) 
neuro-ophthalmologic disorders in, (Clinical Volume 5, Chapter 32) 
Horner’s syndrome, (Clinical Volume 5, Chapter 32) 
myasthenia gravis, (Clinical Volume 5, Chapter 32) 
pre-eclampsia
cortical vision loss in, (Clinical Volume 5, Chapter 32) 
eclampsia, cortical vision loss in, (Clinical Volume 5, Chapter 32) 
noninfectious uveitis, (Clinical Volume 5, Chapter 32) 
occlusive vascular disorders in, (Clinical Volume 5, Chapter 32) 
ophthalmic medications, (Clinical Volume 5, Chapter 32) 
glaucoma medications, (Clinical Volume 5, Chapter 32) 
photodynamic therapy, (Clinical Volume 5, Chapter 32) 
topical anesthetic, dilating drops, (Clinical Volume 5, Chapter 32) 
topical antibiotics, antivirals, (Clinical Volume 5, Chapter 32) 
topical steroids, (Clinical Volume 5, Chapter 32) 
optic nerve in, (Clinical Volume 5, Chapter 32) 
multiple sclerosis, (Clinical Volume 5, Chapter 32) 
optic neuropathies in, (Clinical Volume 5, Chapter 32) 
perinatal ophthalmology and, (Clinical Volume 5, Chapter 39) 
preexisting conditions, (Clinical Volume 5, Chapter 32) 
protein S deficiency and, (Clinical Volume 5, Chapter 23) 
pseudotumor cerebri in, (Clinical Volume 2, Chapter 5) 
pseudoxanthoma elasticum and, (Clinical Volume 5, Chapter 32) 
retinal
choroidal changes, (Clinical Volume 5, Chapter 32) 
choroidal disorders in, (Clinical Volume 5, Chapter 32) 
amniotic fluid embolism, (Clinical Volume 5, Chapter 32) 
central serous chorioretinopathy, (Clinical Volume 5, Chapter 32) 
disseminated intravascular coagulation, (Clinical Volume 5, Chapter 32) 
occlusive vascular disorders, (Clinical Volume 5, Chapter 32) 
pre-eclampsia
choroidopathy in, (Clinical Volume 5, Chapter 32) 
pre-eclampsia and eclampsia, (Clinical Volume 5, Chapter 32) 
choroidopathy in, (Clinical Volume 5, Chapter 32) 
retinal artery occlusion, (Clinical Volume 5, Chapter 32) 
retinal vein occlusion, (Clinical Volume 5, Chapter 32) 
thrombotic thrombocytopenic purpura, (Clinical Volume 5, Chapter 32) 
retinal artery occlusion in, (Clinical Volume 5, Chapter 32) 
retinal diagnostic testing, (Clinical Volume 5, Chapter 32) 
fluorescein angiography, (Clinical Volume 5, Chapter 32) 
indocyanine green angiography, (Clinical Volume 5, Chapter 32) 
retinal disorders, (Clinical Volume 5, Chapter 32) 
retinal vein occlusion in, (Clinical Volume 5, Chapter 32) 
retinitis pigmentosa in, (Clinical Volume 5, Chapter 32) 
rubella. (See Rubella)
toxoplasmic retinochoroiditis, (Clinical Volume 5, Chapter 32) 
transient cerebral blindness in, (Clinical Volume 2, Chapter 7) 
Pregnancy-associated plasma protein-A, beta-human chorionic gonadotropin, (Foundations Volume 3, Chapter 56) 
Prejunctional receptors, (Foundations Volume 3, Chapter 26) 
Premacular gliosis. See Epiretinal membranes
Premacular membranes, (Clinical Volume 3, Chapter 39) (Clinical Volume 6, Chapter 51) See also Vitreous, membranes
Premalignant tumors, (Foundations Volume 3, Chapter 7) 
Prematurity
retinopathy of. (See Retinopathy of prematurity (retrolental fibroplasia))
surgery in infant, (Clinical Volume 6, Chapter 80) 
Prematurity, retinopathy of, (Foundations Volume 1, Chapter 16) 
Premedication, for anesthesia in children, (Clinical Volume 6, Chapter 81) 
Prenatal diagnoses, (Foundations Volume 3, Chapter 56) 
alpha-fetoprotein P X-tra/triple screen test, (Foundations Volume 3, Chapter 56) 
alpha-fetoprotein tetra/quad screen, (Foundations Volume 3, Chapter 56) 
chorionic villus sampling, (Foundations Volume 3, Chapter 56) 
first trimester ultrasound, (Foundations Volume 3, Chapter 56) 
genetic counseling/preconception counseling, (Foundations Volume 3, Chapter 56) 
magnetic resonance imaging, (Foundations Volume 3, Chapter 56) 
maternal screening, (Foundations Volume 3, Chapter 56) 
pregnancy-associated plasma protein-A, beta-human chorionic gonadotropin, (Foundations Volume 3, Chapter 56) 
second trimester ultrasound, (Foundations Volume 3, Chapter 56) 
serum alpha-fetoprotein, (Foundations Volume 3, Chapter 56) 
three-dimensional ultrasound, (Foundations Volume 3, Chapter 56) 
Prepresbyopia, Fresnel lenses in, (Clinical Volume 1, Chapter 52) 
Preretinal neovascularization, in sickle cell disease, (Clinical Volume 3, Chapter 17) See also Sickle cell disease
Preretinal retraction. See Vitreoretinopathy, proliferative
Preseptal space, cellulitis, (Clinical Volume 4, Chapter 25) See also Cellulitis, preseptal
Preservatives
in contact lens care systems, and infection prevention, (Foundations Volume 2, Chapter 80) 
side effects, in infants and children, (Foundations Volume 3, Chapter 43) 
Pressure
on eye, intraocular pressure and, (Foundations Volume 2, Chapter 7) 
in glaucomatolytic crisis
increased, in newborn, (Clinical Volume 3, Chapter 51) 
measurements. (See Tonography; Tonometry)
and mechanism of hypertension, (Clinical Volume 3, Chapter 41) 
tonography. (See Tonography, in glaucoma)
intracranial. (See Intracranial pressure increase)
intraocular. (See Intraocular pressure)
optic nerve damage in, (Clinical Volume 3, Chapter 48) 
Pressure bandages, orbitocranial trauma and, (Clinical Volume 2, Chapter 5) 
Presumed ocular histoplasmosis syndrome (POHS), (3) 13: 26–27; 38: 13; See also Histoplasmosis
choroidal neovascular membranes in, (Clinical Volume 6, Chapter 56) 
fluorescein angiography in, (Clinical Volume 4, Chapter 57) 
HLA antigen association of, (Foundations Volume 2, Chapter 38) 
Pretectal nuclei, optic nerve and, (Foundations Volume 2, Chapter 21) 
Pretectum, pupillary light reflex integration at, (Foundations Volume 2, Chapter 9) 
Prevalence, defined, (Foundations Volume 2, Chapter 43) 
Preventive medicine, occupational ophthalmology and, (Clinical Volume 5, Chapter 47) 
Preventive ophthalmology. See Geographic and preventive ophthalmology
Primary acquired nasolacrimal duct obstruction (PANDO), (Clinical Volume 4, Chapter 13) 
Primary angle-closure glaucoma, (Clinical Volume 6, Chapter 15) 
Primary focal point, (Clinical Volume 1, Chapter 30) 
Primary hyperoxaluria type I, (Clinical Volume 5, Chapter 31) 
Primary immunodeficiency diseases, (Clinical Volume 5, Chapter 40) 
Primary malignancy, metastatic cancer to eye and adnexa and, (Clinical Volume 5, Chapter 34) 
Primary ocular diseases, cataract from, (Clinical Volume 1, Chapter 73) 
Primary phagocytic dysfunction, (Clinical Volume 5, Chapter 40) 
Primed lymphocyte typing, of class II HLA antigens, (Foundations Volume 2, Chapter 38) 
Primidone, ocular toxicity, (Clinical Volume 5, Chapter 37) 
Primitive neuroectodermal tumors, orbital, (Clinical Volume 2, Chapter 41) 
Principal planes, in ray sketching, (Clinical Volume 1, Chapter 30) 
Principal points, in ray sketching, (Clinical Volume 1, Chapter 30) 
Prismatic effects, in bifocals, (Clinical Volume 1, Chapter 44) 
Prism ballast
front toric lens fitting, (Clinical Volume 1, Chapter 54) 
Prism ballasted contact lens, (Clinical Volume 1, Chapter 55) 
Prism(s), (Clinical Volume 1, Chapter 30) 
appropriate power, vector calculation of, (Clinical Volume 1, Chapter 30) 
base-in, Fresnel membrane, (Clinical Volume 1, Chapter 52) 
base position, vector calculation of, (Clinical Volume 1, Chapter 30) 
deviations produced by, (Clinical Volume 1, Chapter 30) 
glass, comparison with Fresnel prisms, (Clinical Volume 1, Chapter 52) 
vertical phoria and, (Clinical Volume 1, Chapter 44) 
Prism techniques
for AC/A determinations, (Clinical Volume 1, Chapter 7) 
in alternate cover tests, (Clinical Volume 1, Chapter 6) 
in base-out test, (Clinical Volume 1, Chapter 14) 
for fusional convergence amplitude, (Clinical Volume 1, Chapter 7) 
for fusional divergence amplitude, (Clinical Volume 1, Chapter 7) 
in monofixation syndrome, (Clinical Volume 1, Chapter 14) 
in red filter test, (Clinical Volume 1, Chapter 6) 
for vertical fusional vergence amplitude, (Clinical Volume 1, Chapter 7) 
Pro-agents, bioinequivalence and, (Foundations Volume 3, Chapter 22) 
Proapoptotic protein BAD, and glaucoma, (Clinical Volume 3, Chapter 57) 
Probability plots, in field defect identification, (Clinical Volume 2, Chapter 2) (Clinical Volume 3, Chapter 49) 
Probenecid, in gonococcal conjunctivitis, (Clinical Volume 4, Chapter 5) 
Prochlorperazine, ocular toxicity, (Clinical Volume 5, Chapter 37) 
Progressive addition lenses (PALs), history of, (Clinical Volume 1, Chapter 44) 
Progressive bifocal chorioretinal atrophy, (Clinical Volume 4, Chapter 66) 
Progressive cone-rod dystrophies, (Clinical Volume 3, Chapter 9) 
Progressive external ophthalmoplegia. See Ophthalmoplegia, progressive external
Progressive hemifacial atrophy, (Foundations Volume 1, Chapter 37) (Clinical Volume 2, Chapter 8) See Parry–Romberg syndrome
Progressive systemic sclerosis. See Scleroderma
Proliferative vitreoretinopathy, (Foundations Volume 2, Chapter 11) See also Retinopathy, (Clinical Volume 3, Chapter 39) See also Retinopathy, proliferative, proliferative; Vitreoretinopathy
retinal detachment with, vitrectomy in, (Clinical Volume 6, Chapter 56) 
retinal pigment epithelium in, (Foundations Volume 1, Chapter 21) 
vitreous fibers and, (Foundations Volume 1, Chapter 16) 
vitreous surgery in, (Clinical Volume 6, Chapter 58 ) 
Promethazine
for acute vestibular neuritis, (Clinical Volume 2, Chapter 18) 
PROMM. See Proximal myotonic myopathy
Propamidine, in Acanthamoeba keratitis, (Foundations Volume 2, Chapter 66) 
Proparacaine
in corneal anesthesia
for antibiotic injection, (Clinical Volume 4, Chapter 26) 
for specimen collection, (Clinical Volume 4, Chapter 18) 
systemic toxicity, (Clinical Volume 5, Chapter 37) 
Proparacaine hydrochloride, (Foundations Volume 3, Chapter 43) 
Propine. See Dipivefrin
Propionibacterium acnes, (Clinical Volume 4, Chapter 24) 
Propionibacterium acnes, infectious endophthalmitis and, (Foundations Volume 2, Chapter 48) 
Propofol
dosage and administration of, for children, (Clinical Volume 6, Chapter 81) 
in lacrimal surgery, (Clinical Volume 6, Chapter 1) 
Propositus, defined, (Foundations Volume 3, Chapter 51) 
Propoxycaine, ocular toxicity, (Clinical Volume 5, Chapter 37) 
Propranolol. See also Beta-adrenergic antagonists
in migraine prophylaxis, (Clinical Volume 2, Chapter 16) 
Proptosis. See also Exophthalmos
in Albright’s disease, (Clinical Volume 5, Chapter 29) 
in aneurysmal bone cyst, (Clinical Volume 2, Chapter 27) 
in Apert’s disease, (Clinical Volume 5, Chapter 29) 
childhood, 2, (Clinical Volume 2, Chapter 14) 
acute, (Clinical Volume 2, Chapter 27 ) 
in aneurysmal bone cyst, (Clinical Volume 2, Chapter 27) 
in Burkitt’s lymphoma, (Clinical Volume 2, Chapter 27) 
in capillary hemangioma, (Clinical Volume 2, Chapter 27) 
computed tomography in, (Clinical Volume 2, Chapter 27) 
differential diagnosis, 2, (Clinical Volume 2, Chapter 27) 
in eosinophilic granuloma, (Clinical Volume 2, Chapter 27) 
in inflammatory pseudotumor, (Clinical Volume 2, Chapter 27) 
magnetic resonance imaging of, (Clinical Volume 2, Chapter 27) 
in metastatic disease, (Clinical Volume 2, Chapter 27) 
in neuroblastoma, (Clinical Volume 2, Chapter 27) 
in sickle cell disease, (Clinical Volume 2, Chapter 27) 
in traumatic orbital hematoma, (Clinical Volume 2, Chapter 27) 
congenital, causes of, (Clinical Volume 2, Chapter 27) 
in craniofacial syndromes, (Clinical Volume 6, Chapter 110) 
in eosinophilic granuloma, (Clinical Volume 2, Chapter 27) 
in Ewing’s sarcoma, (Clinical Volume 2, Chapter 27) 
in hemangioma, capillary, (Clinical Volume 2, Chapter 27) 
lacrimal fossa lesion and, (Clinical Volume 2, Chapter 24) 
mesenchymal tumor and, (Clinical Volume 2, Chapter 24) 
in neuroblastoma, (Clinical Volume 2, Chapter 27) 
in posterior scleritis, (Clinical Volume 2, Chapter 28) 
in sickle cell disease, (Clinical Volume 2, Chapter 27) 
subtle degrees of, (Clinical Volume 2, Chapter 14) 
with true orbital pain, (Clinical Volume 2, Chapter 14) 
in WIlms’ tumor, (Clinical Volume 2, Chapter 27) 
Propylargylamines, antiapoptotic properties, (Clinical Volume 3, Chapter 57) 
Propylthiouracil (PTU), for thyroid disease, (Clinical Volume 2, Chapter 36) 
Prospective worker, occupational ophthalmology and, (Clinical Volume 5, Chapter 47) 
Prostaglandin analogs
Prostaglandin analogues, intraocular pressure, (Foundations Volume 3, Chapter 25) 
Prostaglandins
aqueous humor drainage, (Clinical Volume 3, Chapter 45) 
aqueous humor outflow and, (Foundations Volume 3, Chapter 25) 
inhibitors. (See Nonsteroidal anti-inflammatory drugs (NSAIDs))
intraocular pressure and, (Foundations Volume 2, Chapter 7) 
Prostaglandin synthesis inhibitors
effects on ocular inflammatory disease, (Foundations Volume 2, Chapter 31) 
in ocular inflammation, (Foundations Volume 2, Chapter 31) 
Prostate surgery, blindness after, (Clinical Volume 2, Chapter 5) 
Prosthesis. See Implants; Keratoprosthesis
Prosthesis, infections due to, (Foundations Volume 2, Chapter 53) 
Prosthokeratoplasty. See Keratoplasty; Keratoprosthesis
Prostigmin (neostigmine) test, in myasthenia, (Clinical Volume 2, Chapter 12) 
Protanomalous trichomats, (Foundations Volume 2, Chapter 19) 
Proteases
cataract risk reduction and, (Clinical Volume 1, Chapter 72C) 
neutral, in ocular allergy, (Foundations Volume 2, Chapter 37) 
Protection of eye, (Clinical Volume 3, Chapter 31) 
Protective Eyewear Certification Council (PECC), (Clinical Volume 5, Chapter 45) 
Protein binding
pharmacokinetics and, (Foundations Volume 3, Chapter 23) 
Protein C
Proteinosis, lipoid, lid and periorbital manifestations, (Foundations Volume 3, Chapter 7) 
Protein(s). See also specific proteins
adsorption onto contact lenses, in giant papillary conjunctivitis, (Clinical Volume 4, Chapter 9A) 
in amyloid deposits, (Clinical Volume 2, Chapter 35) 
in cytologic examination, (Foundations Volume 2, Chapter 40) 
deficiency, in xerophthalmia, (Clinical Volume 5, Chapter 59) 
noncollagenous, vitreous, (Foundations Volume 1, Chapter 16) 
noncollagenous structural, vitreous and, (Clinical Volume 3, Chapter 38) 
retinoblastoma gene product, (Clinical Volume 6, Chapter 75) 
visual transduction and, (Foundations Volume 2, Chapter 12) 
Protein S deficiency, 4, (Clinical Volume 5, Chapter 23) 
Proteogylcans, zonular, (Foundations Volume 1, Chapter 14) 
Proteolytic enzymes
in bacterial infections
gram-negative bacilli, (Foundations Volume 2, Chapter 52) 
Proteomic analysis
retinal pigment epithelium, (Foundations Volume 1, Chapter 21) 
Proteomics
Proteus
blepharitis from, (Clinical Volume 4, Chapter 22) 
corneal ulcers from, (Clinical Volume 4, Chapter 18) 
Prothrombin
variant 20210a, detection, (Clinical Volume 5, Chapter 23) 
Protopam. See Pralidoxime
Prototheca wickerhamii, (Foundations Volume 2, Chapter 54) 
Protozoa, (Foundations Volume 2, Chapter 41) (Foundations Volume 2, Chapter 79) See also specific type
infections caused by, (Foundations Volume 2, Chapter 79) See also specific infections
retinitis pigmentosa and, (Foundations Volume 3, Chapter 13) 
Protriptyline, ocular toxicity, (Clinical Volume 5, Chapter 37) 
Provisc. See Viscoelastic materials
Provocative testing, muscarinic antagonists and, (Foundations Volume 3, Chapter 26) 
Proximal myotonic myopathy (PROMM), (Clinical Volume 5, Chapter 28) 
Pruritus
in dermatitis herpetiformis, (Clinical Volume 5, Chapter 27) 
in vernal keratoconjunctivitis, (Clinical Volume 4, Chapter 9) 
Pseudoabducens palsy, (Clinical Volume 2, Chapter 12) 
Pseudoaccommodation, (Clinical Volume 1, Chapter 68) 
Pseudoadenomatous hyperplasia, (Foundations Volume 3, Chapter 11) 
Pseudo Argyll Robertson pupil, (Clinical Volume 2, Chapter 12) 
Pseudobulbar palsy, (Clinical Volume 2, Chapter 8) 
Pseudocarcinomatous hyperplasia, of eyelids, (Clinical Volume 4, Chapter 3) 
Pseudocyst, toxoplasmosis and, (Foundations Volume 3, Chapter 4) 
Pseudocysts, macular, hereditary, (Clinical Volume 3, Chapter 9) 
Pseudodendriform keratitis, (Clinical Volume 4, Chapter 20) 
Pseudodendrites, in herpes zoster keratouveitis, (Clinical Volume 4, Chapter 39) 
Pseudo-Duane retraction syndrome, (Clinical Volume 1, Chapter 20) 
Pseudoexfoliation syndrome, (Clinical Volume 3, Chapter 54B) See also Exfoliation syndrome; (Foundations Volume 1, Chapter 10) (Foundations Volume 3, Chapter 12) 
muscarinic antagonists and, (Foundations Volume 3, Chapter 26) 
Pseudoexophthalmos, (Clinical Volume 2, Chapter 14) 
Pseudofacility, (Foundations Volume 2, Chapter 7) 
outflow measurement and, (Foundations Volume 2, Chapter 7) 
Pseudogerontoxon, in vernal keratoconjunctivitis, (Clinical Volume 4, Chapter 2) 
Pseudoglands of Henle, (Foundations Volume 1, Chapter 29) 
Pseudoglaucoma, optic disc, (Clinical Volume 2, Chapter 5) 
Pseudoglioma. See also Persistent hyperplastic primary vitreous (PHPV); Retrolental fibroplasia (RLF)
differential diagnosis of retinoblastoma and, (Foundations Volume 3, Chapter 21) 
Pseudohistoplasmosis, (Clinical Volume 4, Chapter 48) 
Pseudohypertelorism, (Clinical Volume 5, Chapter 29) 
Pseudohyphae, hyphae versus, (Foundations Volume 2, Chapter 54) 
Pseudohypoparathyroidism, (Clinical Volume 5, Chapter 21) 
Pseudoinflammatory macular dystrophy, (1)60: 8
fluorescein angiography, (Foundations Volume 2, Chapter 113B) 
Pseudoisochromatic plates, in color vision testing, (Clinical Volume 2, Chapter 2) (Clinical Volume 3, Chapter 6) 
in cerebral achromatopsia, (Clinical Volume 2, Chapter 7) 
Pseudomeningocele, (Clinical Volume 2, Chapter 24) 
Pseudomonas, (Foundations Volume 2, Chapter 28)  (Foundations Volume 2, Chapter 52) 
antibiotic resistance, (Foundations Volume 2, Chapter 64) 
chemotherapy. (See Drugs, antimicrobial and antibiotic)
control, microbiology laboratory and, (Foundations Volume 2, Chapter 47) 
in corneal infections, (Foundations Volume 2, Chapter 42) 
contact lenses and, (1)64: 9
corticosteroids in, (Foundations Volume 3, Chapter 31) 
diagnosis, microscopy in, (Foundations Volume 2, Chapter 40 ) 
global impact, (Foundations Volume 2, Chapter 43) See also Epidemiology, of ocular infections
human papillomavirus and, (Foundations Volume 2, Chapter 95) 
laboratory diagnosis, (Foundations Volume 2, Chapter 40) See also specific procedures
microbial component detection, (Foundations Volume 2, Chapter 40) 
ocular teratogenicity, (Foundations Volume 1, Chapter 39) 
polymicrobial, keratitis and, (Foundations Volume 2, Chapter 53) 
postoperative intraocular, organisms causing, (Foundations Volume 3, Chapter 36) 
punctate
superficial, Thygeson’s, (Foundations Volume 3, Chapter 9) 
side effects and toxicity, (Foundations Volume 3, Chapter 42) 
storage and transport, (Foundations Volume 2, Chapter 12) 
ulcerative, (Foundations Volume 2, Chapter 42) 
contact lenses and, (Foundations Volume 2, Chapter 53) 
antimicrobial prophylaxis, (Foundations Volume 2, Chapter 64) 
Pseudomonas, blepharitis from, (Clinical Volume 4, Chapter 22) 
Pseudomonas aeruginosa, keratitis from, (Clinical Volume 4, Chapter 18) 
contact lens-related, (Clinical Volume 4, Chapter 27) 
Pseudopemphigoid, (Clinical Volume 4, Chapter 2) 
Pseudophakia
after cataract surgery, (Foundations Volume 3, Chapter 6) 
anterior chamber, intraocular lens and, (Foundations Volume 3, Chapter 6) 
intraoperative lens implantation in
ametropia as goal of, (Clinical Volume 1, Chapter 68) 
emmetropia as goal of, (Clinical Volume 1, Chapter 68) 
macular edema in, diabetic retinopathy versus, (Foundations Volume 2, Chapter 113D) 
Nd: YAG laser use in, (Clinical Volume 6, Chapter 10 ) 
penetrating keratoplasty for, (Clinical Volume 6, Chapter 26) 
scleral buckling in, (Clinical Volume 6, Chapter 59) 
solar damage and, (Clinical Volume 5, Chapter 55) 
Pseudophakia/pupillary block, (Clinical Volume 3, Chapter 55) 
Pseudophakic cystoid macular edema, (Foundations Volume 2, Chapter 11) 
Pseudophakic dysphotopsia, (Clinical Volume 6, Chapter 11) 
Pseudophakic intraocular lens, (Clinical Volume 6, Chapter 11) 
adjustable-power pseudophakic intraocular lenses, (Clinical Volume 6, Chapter 11) 
Light-Adjustable lens, (Clinical Volume 6, Chapter 11) 
aniridia intraocular lenses, (Clinical Volume 6, Chapter 11) 
aspheric intraocular lenses, (Clinical Volume 6, Chapter 11) 
AcrySof Higher Order Aberration WF Series, (Clinical Volume 6, Chapter 11) 
Sofflex Advanced Optics, (Clinical Volume 6, Chapter 11) 
implantable miniature telescope, (Clinical Volume 6, Chapter 11) 
light-normalizing intraocular lenses, (Clinical Volume 6, Chapter 11) 
Akkommodative ICU, (Clinical Volume 6, Chapter 11) 
BioComFold Intraocular Lens, (Clinical Volume 6, Chapter 11) 
low/high diopter intraocular lenses, (Clinical Volume 6, Chapter 11) 
multifocal intraocular lenses, (Clinical Volume 6, Chapter 11) 
Array Multizonal Refractive intraocular lens, (Clinical Volume 6, Chapter 11) 
optical multifocal intraocular lenses, (Clinical Volume 6, Chapter 11) 
pseudoaccommodative intraocular lenses, (Clinical Volume 6, Chapter 11) 
Toric intraocular lenses, (Clinical Volume 6, Chapter 11) 
AcrySof Toric intraocular lens, (Clinical Volume 6, Chapter 11) 
Artisan Toric Intraocular Lens, (Clinical Volume 6, Chapter 11) 
C-flex Toric Intraocular Lens, (Clinical Volume 6, Chapter 11) 
STAAR Toric lenses, (Clinical Volume 6, Chapter 11) 
for very small incisions, (Clinical Volume 6, Chapter 11) 
UltraChoice Thin Lens, (Clinical Volume 6, Chapter 11) 
Pseudopigmentary glaucoma, (Clinical Volume 3, Chapter 54G) 
Pseudoplasticity, viscoelastic agents, (Clinical Volume 6, Chapter 9) 
Pseudoprolactinomas, (Clinical Volume 2, Chapter 6) 
Pseudo-pseudohypoparathyroidism, (Clinical Volume 5, Chapter 21) 
Pseudoretention cysts, (Foundations Volume 1, Chapter 29) 
Pseudoretinoblastoma, (Clinical Volume 4, Chapter 53) See Pseudoglioma
Pseudosarcomatous fasciitis. See Fasciitis, nodular
Pseudotumor, orbital
clinical features of, (Foundations Volume 3, Chapter 17) 
corticosteroids in, (Foundations Volume 3, Chapter 31) 
Pseudotumor cerebri, pediatric, 45–46
Pseudo-von Graefe sign
in oculomotor synkinesis, (Clinical Volume 2, Chapter 12) 
in parasellar syndromes, (Clinical Volume 2, Chapter 12) 
Psoralen-ultraviolet A (PUVA) therapy, cataract from, (Clinical Volume 1, Chapter 73) 
Psychedelic agents, ocular toxicity, (Clinical Volume 5, Chapter 37) 
Psychiatric disorders, gangliosidosis and, (Foundations Volume 3, Chapter 54B) 
Psychologic counseling, retinitis pigmentosa and, (Clinical Volume 3, Chapter 24) 
Psychologic factors
in atopic dermatitis, (Clinical Volume 5, Chapter 27) 
in patient preparation, for anesthesia in child, (Clinical Volume 6, Chapter 80 ) 
in perimetric testing, (Clinical Volume 3, Chapter 49) 
Psychopharmaceutical agents, ocular teratogenicity, (Foundations Volume 1, Chapter 39) 
Psychophysical abnormalities, in diabetic retinopathy, (Clinical Volume 3, Chapter 30) 
Psychophysics
eye movements. (See Ocular motility, psychophysics ofof)
Pteroylglutamic acid. See Folic acid
Pterygium, (Foundations Volume 1, Chapter 29) (Foundations Volume 3, Chapter 8) (Clinical Volume 4, Chapter 16) (Clinical Volume 6, Chapter 35) (Clinical Volume 6, Chapter 9) 
beta radiation therapy in, (Clinical Volume 6, Chapter 35) 
conjunctival autograft in, (Clinical Volume 6, Chapter 35) 
corticosteroids in, (Clinical Volume 6, Chapter 35) 
differential diagnosis, (Clinical Volume 6, Chapter 35) 
excision
bare sclera technique, (Clinical Volume 6, Chapter 35) 
laser therapy with, (Clinical Volume 6, Chapter 35) 
with primary closure, (Clinical Volume 6, Chapter 35) 
head, transplantation, (Clinical Volume 6, Chapter 35) 
histologic characteristics, (Clinical Volume 6, Chapter 35) 
light toxicity and, (Foundations Volume 2, Chapter 15) 
limbal autograft in, (Clinical Volume 6, Chapter 35) 
Pterygopalatine ganglion, (Clinical Volume 2, Chapter 40) 
PTFE. See Polytetrafluoroethylene (PTFE)
Ptosis, (Foundations Volume 1, Chapter 5) (Foundations Volume 3, Chapter 53) (Clinical Volume 2, Chapter 3) (Clinical Volume 2, Chapter 8) (Clinical Volume 2, Chapter 14) See also Blepharoptosis, 22
after conjunctival flap, (Clinical Volume 6, Chapter 33) 
after lid repair, (Clinical Volume 5, Chapter 75) 
after radial keratotomy, (Clinical Volume 6, Chapter 41) 
congenital aponeurotic, (Clinical Volume 5, Chapter 78) 
congenital myogenic, (Clinical Volume 5, Chapter 78) 
corticosteroids and, (Foundations Volume 3, Chapter 31) 
craniofacial anomalies and, (Foundations Volume 1, Chapter 41) 
in craniofacial syndromes, (Clinical Volume 6, Chapter 110) 
in generalized fibrosis syndrome, (Clinical Volume 1, Chapter 20) 
in Graves’ disease, (Clinical Volume 5, Chapter 81) 
in Horner’s syndrome, (Clinical Volume 2, Chapter 15) 
in Marfan’s syndrome, (Clinical Volume 5, Chapter 29) 
in myotonic dystrophy, (Foundations Volume 3, Chapter 58) 
in progressive external ophthalmoplegia, (Clinical Volume 1, Chapter 20) 
surgery, (Clinical Volume 5, Chapter 75) (Clinical Volume 5, Chapter 78)  (Clinical Volume 5, Chapter 81) 
alloplastic materials, (Clinical Volume 5, Chapter 88) 
in anophthalmic socket, (Clinical Volume 5, Chapter 83) 
anterior levator resection, (Clinical Volume 5, Chapter 78) 
contraindications, (Clinical Volume 6, Chapter 110) 
in craniofacial syndromes, (Clinical Volume 6, Chapter 110) 
examination of ptosis patient, (Clinical Volume 5, Chapter 78) 
external approach to, (Clinical Volume 5, Chapter 78) 
external tarsal aponeurectomy, (Clinical Volume 5, Chapter 78) 
Fasanella-Servat, (Clinical Volume 5, Chapter 78) 
fascial sling/silicone procedures, (Clinical Volume 5, Chapter 83) 
indications, 5; , (6) 110: 18–19
maximal anterior levator resection, (Clinical Volume 5, Chapter 78) 
patients with eye-protective mechanisms, (Clinical Volume 5, Chapter 78) 
postoperative care, (Clinical Volume 5, Chapter 78) 
tarsal-Muller’s muscle resection, (Clinical Volume 5, Chapter 78) 
PTU. See Propylthiouracil (PTU)
P53 tumor suppressor protein, and apoptotic signaling, (Clinical Volume 3, Chapter 57) 
Public health. See Epidemiology
Pulfrich stereo phenomenon, in optic neuritis, (Clinical Volume 2, Chapter 5) 
Pullularia pullulans, (Foundations Volume 2, Chapter 54) 
Pulmonary disorders. See Lung disease
Pulmonary 2-receptors, blockage, topical -blockers and, (Foundations Volume 3, Chapter 40) 
Pulse electroretinogram, (Clinical Volume 3, Chapter 2) 
Pulse train, saccadic, (Clinical Volume 2, Chapter 11) 
Pulverulent cataract, central, (Foundations Volume 1, Chapter 15) 
Pulvinar nucleus, retinal projection to, (Clinical Volume 2, Chapter 4) 
Pumetate inner choroidopathy, (Clinical Volume 4, Chapter 49) 
Punctal lacerations, (Clinical Volume 5, Chapter 75) 
Punctate epithelial erosions, (Clinical Volume 4, Chapter 17) 
Punctate epithelial microcysts, (Clinical Volume 4, Chapter 17) 
Punctate keratitis
onchocerciasis and, (Clinical Volume 5, Chapter 62) 
sclerosing, onchocerciasis and, (Clinical Volume 5, Chapter 62) 
Punctate keratopathy, (Clinical Volume 4, Chapter 17) 
conjunctival response with, (Clinical Volume 4, Chapter 17) 
epithelial, (Clinical Volume 4, Chapter 17) 
contact lens-associated, (Clinical Volume 4, Chapter 27) 
lid disease with, (Clinical Volume 4, Chapter 17) 
Punctum, atresia of, (Foundations Volume 3, Chapter 7) 
Pupillary block, angle-closure glaucoma caused by, (Clinical Volume 3, Chapter 55) 
Pupillary light response, neuro-ophthalmologic examination, (Clinical Volume 2, Chapter 10) 
Pupillary membrane
persistent, (1)53: 18
Pupillary ruff, 4, (Clinical Volume 4, Chapter 31) 
Pupillary zone, 4, (Clinical Volume 4, Chapter 31) 
Pupillography, computerized infrared, for afferent pupil defect, (Clinical Volume 2, Chapter 15) 
Pupilloplasty, laser, (Clinical Volume 3, Chapter 53) 
Pupil of eye, (Clinical Volume 2, Chapter 15 ) 
aberrant regeneration pupil, (Clinical Volume 2, Chapter 15) 
Adie’s, light-near dissociation, (Clinical Volume 2, Chapter 15) 
Argyll Robertson, (Clinical Volume 2, Chapter 15) 
block
after glaucoma surgery, (Clinical Volume 6, Chapter 24) 
angle-closure glaucoma due to, (Clinical Volume 3, Chapter 53) (Clinical Volume 3, Chapter 54E) 
after cataract surgery, (Clinical Volume 3, Chapter 54G) 
after penetrating keratoplasty, (Clinical Volume 6, Chapter 26) 
microspherophakia and, (Clinical Volume 3, Chapter 51) 
in anterior chamber IOL implantation, (Clinical Volume 6, Chapter 8) 
cataract surgery and, (Clinical Volume 3, Chapter 54G) 
differential diagnosis, (Clinical Volume 3, Chapter 53) 
intraocular lens implantation and, (Clinical Volume 3, Chapter 54G) 
malignant glaucoma versus, (Clinical Volume 3, Chapter 53) 
relative, in angle-closure glaucoma, (Clinical Volume 3, Chapter 53) 
reverse, in pigment dispersion syndrome, (Clinical Volume 3, Chapter 54B) 
border of, gonioscopy of, (Clinical Volume 3, Chapter 44) 
characteristics of, (Clinical Volume 2, Chapter 15) 
diameter, perimetric testing and, (Clinical Volume 3, Chapter 49) 
dilation
in angle-closure glaucoma, (Clinical Volume 3, Chapter 53) 
for cataract surgery, pediatric, (Clinical Volume 6, Chapter 100) 
in exfoliation syndrome, (Clinical Volume 3, Chapter 54B) 
in dorsal midbrain syndrome, (Clinical Volume 2, Chapter 15) 
enlargement
in combined cataract extraction and glaucoma surgery, (Clinical Volume 6, Chapter 16) 
episodic dysfunction, (Clinical Volume 2, Chapter 15) 
examination, in comatose patients, (Clinical Volume 2, Chapter 3) 
in exfoliation syndrome, (Clinical Volume 3, Chapter 54B) 
fixed dilated, pharmacologic accidents, (Clinical Volume 2, Chapter 15) 
function, pupillomotor pathway, 2–3, (Clinical Volume 2, Chapter 15) 
in herpes zoster, (Clinical Volume 4, Chapter 20) 
in Horner’s syndrome, (Clinical Volume 2, Chapter 15) 
in light-near dissociation syndromes, (Clinical Volume 2, Chapter 15) 
light reflex pathway of, (Clinical Volume 2, Chapter 15) 
Marcus Gunn. (See Marcus Gunn phenomenon)
membranes, vitrectomy for, (Clinical Volume 6, Chapter 56) 
miotic, in uveitis, (Clinical Volume 4, Chapter 32) 
oculosympathetic defects, (Clinical Volume 2, Chapter 15) 
oculosympathetic pathways of, (Clinical Volume 2, Chapter 15) 
ophthalmoscopy and, (Clinical Volume 1, Chapter 30) 
orbital disease and, (Clinical Volume 2, Chapter 22) 
paradoxical pupillary response, (Clinical Volume 2, Chapter 15) 
pseudo Argyll Robertson in herpes zoster ophthalmicus, (Clinical Volume 2, Chapter 12) 
relative afferent pupillary defect and, (Clinical Volume 2, Chapter 15) 
in retinal light regulation, (Clinical Volume 1, Chapter 30) 
size, (Clinical Volume 1, Chapter 30) 
anatomic considerations, (Clinical Volume 2, Chapter 15) 
in angle-closure glaucoma, (Clinical Volume 3, Chapter 53) 
depth of field and focus and, (Clinical Volume 1, Chapter 33) 
factors influencing, (Clinical Volume 2, Chapter 15) 
resolving power and, (Clinical Volume 1, Chapter 33) 
sparing, in oculomotor palsy, (Clinical Volume 2, Chapter 12) 
with cavernous sinus lesions, (Clinical Volume 2, Chapter 12) 
“springing, ”, (2) 15: 25
tonic pupil syndrome, (Clinical Volume 2, Chapter 15) 
Wernicke’s hemianopic, (Clinical Volume 2, Chapter 7) 
Pupil(s), (Foundations Volume 1, Chapter 11) (Foundations Volume 2, Chapter 9 ) 
anatomy and physiology, (Foundations Volume 2, Chapter 9) 
diameter, and automated perimetry, (Foundations Volume 2, Chapter 109) 
insensitivity to light, (Foundations Volume 2, Chapter 15) 
movement, properties of light and effect on, (Foundations Volume 2, Chapter 9) 
neuropeptide effects on, (Foundations Volume 2, Chapter 9) 
tonic. (See Adie’s syndrome)
ultrasound biomicroscopy, 2, (Foundations Volume 2, Chapter 106) 
Pupil-supported lenses, (Clinical Volume 6, Chapter 11) 
Purdue visual standards, (Clinical Volume 5, Chapter 47) 
“Pure” microphthalmos. See Nanophthalmia
Purine analogues, immunosuppression using, (Clinical Volume 4, Chapter 2) 
Purkinje effect, color perception and, (Clinical Volume 3, Chapter 6) 
Purkinje-Sanson image, first, (Clinical Volume 1, Chapter 65) 
Purlytin, in photodynamic therapy, (Clinical Volume 1, Chapter 69C) 
Purpura, in pregnancy, (Clinical Volume 5, Chapter 32) 
Purpuric fever, Brazilian, (Clinical Volume 4, Chapter 26) 
Purtscher-like retinopathy
cotton-wool spots in, (Clinical Volume 3, Chapter 14) 
labor and delivery and, (Clinical Volume 5, Chapter 32) 
PUVA therapy. See Psoralen-ultraviolet A (PUVA) therapy
PVEP. See Pattern visual evoked potential
Pyoceles, (Clinical Volume 4, Chapter 13) See also Mucoceles
Pyogenic granuloma-conjunctival cyst, (Clinical Volume 6, Chapter 83) 
Pyramidine analogs, (Foundations Volume 3, Chapter 33) 
Pyrazolones. See Nonsteroidal anti-inflammatory drugs (NSAIDs)
Pyridoxine (vitamin B6)
Pyridoxine (vitamin B6)
Pyrimethamine, in toxoplasmosis, (Clinical Volume 4, Chapter 46) 
Pyrimethamine (Daraprim), in toxoplasmosis, (Foundations Volume 2, Chapter 66) (Foundations Volume 2, Chapter 76) 
4q addition syndrome, (Foundations Volume 3, Chapter 52) 
7q addition syndrome, (Foundations Volume 3, Chapter 52) 
10q addition syndrome, (Foundations Volume 3, Chapter 52) 
13q addition syndrome, (Foundations Volume 3, Chapter 52) 
14q addition syndrome, distal and proximal, (Foundations Volume 3, Chapter 52) 
3q addition syndrome (Cornelia de Lange syndrome), (Foundations Volume 3, Chapter 52) 
13q deletion syndrome, (Foundations Volume 3, Chapter 52) 
retinoblastoma and, (Foundations Volume 3, Chapter 62) 
18q deletion syndrome, (Foundations Volume 3, Chapter 52) 

 Back to Top

Subject Index Q
QELS. See Quasielastic light scattering (QELS)
13q-syndrome, retinoblastoma and, (Clinical Volume 6, Chapter 75) 
Quadrantanopia, striate, (Clinical Volume 2, Chapter 7) 
Quality-adjusted life-years, (Clinical Volume 5, Chapter 69) 
Queensland tick typhus, (Foundations Volume 2, Chapter 58) 
Quickert-Dryden tubes, intubation of lacrimal system, (Clinical Volume 4, Chapter 13) 
Quinacrine, ocular toxicity, (Clinical Volume 5, Chapter 37) 
vortex keratopathy and, (Clinical Volume 4, Chapter 17) 
Quinine, side effects
ocular teratogenicity, (Clinical Volume 5, Chapter 39) 
Quinine urea hydrochloride, in permanent local anesthesia, (Foundations Volume 3, Chapter 35) 

 Back to Top

Subject Index R
Rabies prophylaxis, lid trauma and, (Clinical Volume 5, Chapter 75) 
Rabinowitz indices, (Clinical Volume 1, Chapter 65) 
Race
diabetic retinopathy and, (Clinical Volume 3, Chapter 30) 
ocular trauma and, (Clinical Volume 5, Chapter 56) 
Racemose hemangiomas of retina, thalamus, midbrain, (Clinical Volume 2, Chapter 17) 
Racemouse angioma, (Clinical Volume 2, Chapter 17) 
Racing, automobile, eye injuries from, protective device effectiveness and, (Clinical Volume 5, Chapter 45) 
Racket sports. See also Sports medicine; specific sport
eye injuries from, protective device effectiveness and, (Clinical Volume 5, Chapter 45) 
ocular injuries in, (Clinical Volume 5, Chapter 56) 
Racquetball, eye injuries from, protective device effectiveness and, (Clinical Volume 5, Chapter 45) 
Radial keratotomy, (Clinical Volume 6, Chapter 41 ) 
aberrations after, (Clinical Volume 1, Chapter 30) 
American technique, (Clinical Volume 6, Chapter 41) 
anterior segment surgery after, (Clinical Volume 6, Chapter 41) 
complications, operative, (Clinical Volume 6, Chapter 41) 
double-pass technique, (Clinical Volume 6, Chapter 41) 
history of procedure, (Clinical Volume 6, Chapter 41) 
incisions, (Clinical Volume 6, Chapter 41) 
inaccurate placement, (Clinical Volume 6, Chapter 41) 
transverse incisions couple with, astigmatism and, (Clinical Volume 6, Chapter 42) 
traumatic rupture, (Clinical Volume 6, Chapter 41) 
patient selection, (Clinical Volume 6, Chapter 41) 
rigid gas-permeable lens fitting after, (Clinical Volume 1, Chapter 54) 
new lens designs, (Clinical Volume 1, Chapter 54) 
Russian technique, (Clinical Volume 6, Chapter 41) 
videokeratography in, (Clinical Volume 1, Chapter 65) 
Radial peripapillary capillaries, (Foundations Volume 2, Chapter 5) 
Radiation
cataract caused by, (Clinical Volume 6, Chapter 100) 
geniculocalcarine, (Clinical Volume 2, Chapter 4) 
high-energy, exposure to, cataract risk with, (Clinical Volume 1, Chapter 72C) 
ionizing, cataracts with, (Clinical Volume 1, Chapter 73) 
ocular damage. (See Light toxicity)
phosphenes created by, (Foundations Volume 2, Chapter 20) 
solar. (See also Light toxicity)
ocular protection from, (Clinical Volume 5, Chapter 55 ) 
ultraviolet. (See Ultraviolet radiation)
Radiation retinopathy, photocoagulation in, (Clinical Volume 6, Chapter 76) 
Radiation therapy
canalicular effects, (Clinical Volume 4, Chapter 13) 
of conjunctival tumors, (Clinical Volume 4, Chapter 10) 
corneal degeneration from, (Clinical Volume 4, Chapter 16) 
in craniopharyngioma, (Clinical Volume 2, Chapter 6) 
in dysgerminomas, (Clinical Volume 2, Chapter 6) 
in Langerhans’ cell histiocytosis, (Clinical Volume 2, Chapter 39) 
in malignant melanoma, uveal, (Clinical Volume 6, Chapter 70) 
in metastases to eye and orbit, (Clinical Volume 2, Chapter 46) 
nasolacrimal duct obstruction after, (Clinical Volume 4, Chapter 13) 
in optic neuropathy, (Clinical Volume 2, Chapter 36) 
orbital
in Kaposi’s sarcoma, (Clinical Volume 2, Chapter 37) 
in thyroid orbitopathy, (Clinical Volume 2, Chapter 36) 
pituitary, in adenoma, (Clinical Volume 2, Chapter 6) 
in retinoblastoma, episcleral plaque radiotherapy, (Clinical Volume 6, Chapter 109 ) 
in rhabdomyosarcoma, (Clinical Volume 2, Chapter 43) 
in thyrotoxicosis, (Clinical Volume 5, Chapter 21) 
in vernal keratoconjunctivitis, (Clinical Volume 4, Chapter 9) 
Radiculoneuritis, in Lyme disease, (Foundations Volume 2, Chapter 75) 
Radioactive microspheres, in blood flow determination, (Foundations Volume 2, Chapter 5) 
Radioactive plaque brachytherapy, for posterior uveal melanoma, (Clinical Volume 6, Chapter 70 ) 
relative indications, (Clinical Volume 6, Chapter 70) 
special considerations, (Clinical Volume 6, Chapter 70) 
Radioisotope scans. See Scanning
Radiology, (Clinical Volume 2, Chapter 22) See also specific modalities
in chiasmal syndromes, (Clinical Volume 2, Chapter 6) 
for fetal visualization, (Foundations Volume 3, Chapter 56) 
for ocular measurements, (Clinical Volume 1, Chapter 33) 
in optic nerve disease, acquired, (Clinical Volume 2, Chapter 5) 
in optic neuropathy, carcinomatous, (Clinical Volume 2, Chapter 5) 
of pituitary tumors, (Clinical Volume 2, Chapter 6) 
in pseudotumor cerebri, (Clinical Volume 2, Chapter 5) 
in sphenoidal mucocele, (Clinical Volume 2, Chapter 6) 
“swollen disc, ”, (2) 5: 49–50of
in Wegener’s granulomatosis, (Clinical Volume 2, Chapter 35) 
Radionuclide studies, in uveitis, (Clinical Volume 4, Chapter 37) 
Radionuclide therapy, iodine-131, for thyroid disease, (Clinical Volume 2, Chapter 36) 
Radiotherapy. See Radiation therapy
Raeder paratrigeminal neuralgia, (Foundations Volume 1, Chapter 36) 
Raeder paratrigeminal neuralgia syndrome, (Foundations Volume 1, Chapter 36) (Foundations Volume 1, Chapter 36) 
Raman spectroscopy, (Clinical Volume 3, Chapter 38) 
Ramsay Hunt syndrome, (Foundations Volume 1, Chapter 37) 
Ramsay Hunt syndrome (herpes zoster cephalicus), (Clinical Volume 2, Chapter 8) 
Random dot cinematograms, (Clinical Volume 2, Chapter 7) 
Random-Dot Tests of Motion Perception, (Foundations Volume 2, Chapter 22) 
RANTES protein, inflammation and, (Foundations Volume 2, Chapter 27) 
RAPD (relative afferent pupillary defect), (Foundations Volume 2, Chapter 9) 
Rathke pouch
tumor of. (See Craniopharyngiomas)
RDS locus, heterogeneity, (Clinical Volume 3, Chapter 2) 
Reactive lymphoid hyperplasia, conjunctival, (Foundations Volume 3, Chapter 8) 
Reading
ocular conditions affecting, (Clinical Volume 5, Chapter 42) 
optimal image characteristics for, (Clinical Volume 1, Chapter 46A) 
systemic conditions affecting, (Clinical Volume 5, Chapter 42) 
visual system function and, (Clinical Volume 2, Chapter 2) 
Reading assessment, (Clinical Volume 2, Chapter 7) 
Reading tests
for visual acuity, (Clinical Volume 5, Chapter 51) 
in visual agnosia, (Clinical Volume 2, Chapter 7) 
Real-time quantitative polymerase chain reaction, (Foundations Volume 2, Chapter 40B) 
Rebound nystagmus, (Clinical Volume 2, Chapter 11) 
Rebound phenomenon, inflammatory, corticosteroids and, (Clinical Volume 4, Chapter 19) 
Receptor(s)
bacterial, and host ocular surface, (Foundations Volume 2, Chapter 52) 
for catecholamines, (Foundations Volume 3, Chapter 29) 
HLA disease association and, (Foundations Volume 2, Chapter 38) 
Reciprocal synapses, (Foundations Volume 1, Chapter 19) 
Recklinghausen disease. See Neuofibromatosis
Recombinant DNA technology, (Foundations Volume 1, Chapter 19A) 
Reconstructive surgery
of anterior segment, after surgical repair of traumatic injury, (Clinical Volume 6, Chapter 39) 
of lacrimal drainage system, (Clinical Volume 5, Chapter 79) 
Rectus muscles, (Foundations Volume 1, Chapter 5) (Foundations Volume 1, Chapter 32) 
in Apert’s syndrome, (Foundations Volume 3, Chapter 58) 
computed tomography of, (Clinical Volume 2, Chapter 24) 
inferior
congenital fibrosis, (Clinical Volume 1, Chapter 20) 
in Graves’ orbitopathy, (Clinical Volume 2, Chapter 24) 
in movements of eye, (Clinical Volume 1, Chapter 2) 
in thyroid orbitopathy, (Clinical Volume 2, Chapter 36) 
in thyrotoxicosis ophthalmoplegia, (Clinical Volume 1, Chapter 20) 
isolation, Baerveldt tube implantation and, (Clinical Volume 6, Chapter 17) 
lateral, (Clinical Volume 4, Chapter 31) 
Duane retraction syndrome and, (Clinical Volume 1, Chapter 20) 
in Graves’ orbitopathy, (Clinical Volume 2, Chapter 24) 
isolated enlargement of, (Clinical Volume 2, Chapter 24) 
in myasthenia gravis, (Clinical Volume 1, Chapter 20) 
palsy, saccadic velocity in, (Clinical Volume 1, Chapter 21) 
in strabismus fixus, (Clinical Volume 1, Chapter 20) 
loss during surgery, (Clinical Volume 1, Chapter 20) 
medial
Duane retraction syndrome and, (Clinical Volume 1, Chapter 20) 
in Graves’ orbitopathy, (Clinical Volume 2, Chapter 24) 
loss during surgery, (Clinical Volume 1, Chapter 20) 
in progressive external ophthalmoplegia, (Clinical Volume 1, Chapter 20) 
recession, in Duane’s syndrome, (Clinical Volume 6, Chapter 96) 
slippage during surgery, (Clinical Volume 1, Chapter 20) 
in strabismus fixus, (Clinical Volume 1, Chapter 20) 
in thyrotoxicosis ophthalmoplegia, (Clinical Volume 1, Chapter 20) 
orbital fascial system and, (Foundations Volume 1, Chapter 32) 
proprioception from, (Clinical Volume 1, Chapter 4) 
slippage during surgery, (Clinical Volume 1, Chapter 20) 
superior
in movements of eye, (Clinical Volume 1, Chapter 2) 
surgery, (Clinical Volume 6, Chapter 83) See also Surgery, of rectus muscles
complications of, (Clinical Volume 6, Chapter 83) 
contraindications to, (Clinical Volume 6, Chapter 83) 
in dissociated horizontal deviations, (Clinical Volume 1, Chapter 18) 
in dissociated vertical deviations, (Clinical Volume 1, Chapter 18) 
postoperative care, (Clinical Volume 6, Chapter 83) 
transposition. (See also Surgery, of muscles, transposition)
in Duane’s syndrome, (Clinical Volume 6, Chapter 96) 
saccadic velocity and, (Clinical Volume 1, Chapter 21) 
in thyroid orbitopathy, (Clinical Volume 2, Chapter 36) 
vertical
transposition
in Duane’s syndrome, (Clinical Volume 6, Chapter 96) 
horizontal, in cyclotropia, (Clinical Volume 6, Chapter 97) 
weakening, in Duane’s syndrome, (Clinical Volume 6, Chapter 96) 
Recurrent erosion syndrome, (Foundations Volume 3, Chapter 18) 
Red blood cells, in vitreous, (Foundations Volume 3, Chapter 14) 
Red filter, in amblyopia, (Clinical Volume 1, Chapter 11) 
Redox fluorometry, (Clinical Volume 1, Chapter 31) 
Reduced antibiotic use, antimicrobial resistance and, (Foundations Volume 2, Chapter 65) 
Reduced contrast testing, (Clinical Volume 2, Chapter 2) 
Reduced eye model, (Clinical Volume 1, Chapter 33) 
and retinal image size, (Clinical Volume 1, Chapter 33) 
Reduced illumination, acuity at, (Clinical Volume 2, Chapter 10) 
Reflex blepharospasm, (Foundations Volume 1, Chapter 37) 
Reflex(es). See also Light reflex
fixation. (See Fixation)
fusion. (See Fusion)
gustatory-lacrimal. (See Crocodile tears)
near. (See Near reflex)
oculocephalic. (See Oculocephalic reflex)
oculogyric auricular, (Clinical Volume 2, Chapter 8) 
palpebral-oculogyric, (Clinical Volume 2, Chapter 8) 
pupillary. (See Pupil of eye, light reflex)
tear secretion and, (Clinical Volume 2, Chapter 3) 
vestibulo-colic, (Clinical Volume 1, Chapter 4) 
vestibulo-ocular. (See Vestibulo-ocular reflex)
vestibulo-optokinetic, (Foundations Volume 1, Chapter 38) 
Reflexive saccades, (Foundations Volume 1, Chapter 38) 
Refraction, (Clinical Volume 1, Chapter 30) See also Reflection
axial length of eye and, (Clinical Volume 1, Chapter 34 ) 
binocular balancing, (Clinical Volume 1, Chapter 54) 
cycloplegic. (See Cycloplegic refraction)
distortions
growth of eye and, (Clinical Volume 1, Chapter 34) 
hereditary factors in, (Clinical Volume 1, Chapter 34 ) 
indices of. (See Refractive index)
optical components, (Clinical Volume 1, Chapter 34 ) 
during growth of eye, (Clinical Volume 1, Chapter 34) 
perimetric testing and, (Clinical Volume 3, Chapter 49) 
power of reduced eye, (Clinical Volume 1, Chapter 33) 
reduced vergence and, (Clinical Volume 1, Chapter 33) 
spherical refracting surface, (Clinical Volume 1, Chapter 30) 
mathematical considerations, (Clinical Volume 1, Chapter 30) 
status in newborns, (Clinical Volume 5, Chapter 39) 
Refractive errors. See also specific type
compensation for, (Clinical Volume 1, Chapter 63) 
as complication of rectus muscle surgery, (Clinical Volume 6, Chapter 83) 
indirect-acting muscarinic agonists in, (Foundations Volume 3, Chapter 26) 
occupational ophthalmology and, (Clinical Volume 5, Chapter 47) 
Refractive keratoplasty. See Keratoplasty
Refractive multifocal intraocular lenses, (Clinical Volume 1, Chapter 68A) 
Refractive myopia, (Clinical Volume 1, Chapter 42) 
Refractive state of eye, (Clinical Volume 1, Chapter 33 ) 
accommodation and, (Clinical Volume 1, Chapter 33) 
after scleral buckling, (Clinical Volume 6, Chapter 59) 
aphakia and, (Clinical Volume 1, Chapter 33) See also Aphakia
complications of, after radial keratotomy, (Clinical Volume 6, Chapter 41) 
correction of
after penetrating keratoplasty, in children, (Clinical Volume 6, Chapter 106) 
contact lenses in. (See Contact lenses)
cycloplegic. (See Cycloplegic refraction)
Fresnel lenses in, (Clinical Volume 1, Chapter 52) 
keratomileusis in, (Clinical Volume 6, Chapter 46) See also Keratomileusis
multifocal lenses in, (Clinical Volume 1, Chapter 44) See also Bifocals; Trifocals
spectacle lenses in. (See Spectacle lenses)
surgery in, (Clinical Volume 6, Chapter 41)  (Clinical Volume 6, Chapter 42) See also Surgery, refractive
in diabetes mellitus, (Clinical Volume 5, Chapter 20) 
diurnal fluctuation in, after radial keratotomy, (Clinical Volume 6, Chapter 41) 
low vision. (See Low visionin)
spectacle magnification and, (Clinical Volume 1, Chapter 33) 
Refractive surgery
photophobia associated with, (Foundations Volume 3, Chapter 38) 
Refractive surgery. See Surgery, refractive
Refractometry, spatially resolved, aberration measurement in, (Clinical Volume 1, Chapter 70) 
Refrigeration, in microbiology laboratory, (Foundations Volume 2, Chapter 47) 
Regan-Lancaster dial, with cross cylinder, (Clinical Volume 2, Chapter 38) 
Regeneration
aberrant, of facial nerve, (Foundations Volume 1, Chapter 37) 
in parasympathetic nervous system, (Foundations Volume 2, Chapter 9) 
Rehabilitation, (Clinical Volume 2, Chapter 7) 
after cataract surgery, in pediatric patient, (Clinical Volume 6, Chapter 100) 
after penetrating keratoplasty, in pediatric patient, (Clinical Volume 6, Chapter 106) 
aphakia, with epikeratophakia, (Clinical Volume 6, Chapter 103) See also Epikeratophakiaof
in cerebral visual dysfunction, (Clinical Volume 2, Chapter 7) 
Reis-Bucklers’ corneal dystrophy, (Clinical Volume 4, Chapter 16) 
superficial keratectomy in, (Clinical Volume 6, Chapter 28) 
Relapsing polychondritis, (Clinical Volume 5, Chapter 26) 
Related conditions of lens, lentiglobus, (Clinical Volume 1, Chapter 73) 
Relative afferent pupillary defect, (Clinical Volume 2, Chapter 15) 
Relative afferent pupillary defect (RAPD), (Foundations Volume 2, Chapter 9) 
Releasable sutures, (Clinical Volume 6, Chapter 15) 
Reliability indices (catch-trials), (Clinical Volume 2, Chapter 10) 
Remifentanil, dosage and administration of, for children, (Clinical Volume 6, Chapter 81) 
Renal cell carcinoma, (Clinical Volume 5, Chapter 31) 
Renal disease. See Kidney disease
Renal disease, cataract from, (Clinical Volume 1, Chapter 73) 
Renal-retinal dysplasia, (Clinical Volume 5, Chapter 31) 
Representation of results (graphic display), (Clinical Volume 2, Chapter 10) 
RER. See Rough endoplasmic reticulum
Rescula, intraocular pressure and, (Foundations Volume 2, Chapter 7) 
Rescula (unoprostone), for glaucoma, (Clinical Volume 3, Chapter 56) 
Research
background development in, (Clinical Volume 5, Chapter 66) 
bias effect in, minimization of, (Clinical Volume 5, Chapter 66) 
clinical
cohort studies in, (Clinical Volume 5, Chapter 66) 
data analysis in, biometric methods of, (Clinical Volume 5, Chapter 66) 
diagnostic and therapeutic procedures in, standardization of, (Clinical Volume 5, Chapter 66) 
eligibility and exclusion criteria for, (Clinical Volume 5, Chapter 66) 
epidemiologic approach to, (Clinical Volume 5, Chapter 66 ) 
follow-up length and completeness of, (Clinical Volume 5, Chapter 66) 
general objectives of, development of, (Clinical Volume 5, Chapter 66) 
informed consent for, (Clinical Volume 5, Chapter 66) 
minimization of data collected in, (Clinical Volume 5, Chapter 66) 
minimum number of patients needed for, (Clinical Volume 5, Chapter 66) 
natural history studies in, (Clinical Volume 5, Chapter 66) 
patient explanation in, (Clinical Volume 5, Chapter 66) 
protocol elements in, (Clinical Volume 5, Chapter 66) 
randomized clinical trials in, (Clinical Volume 5, Chapter 66) 
rationale development in, (Clinical Volume 5, Chapter 66) 
risk-benefit ratio in, (Clinical Volume 5, Chapter 66) 
specific questions in, development of, (Clinical Volume 5, Chapter 66) 
statistics in, (Clinical Volume 5, Chapter 67) See also Statistics
studies of cases and controls in, (Clinical Volume 5, Chapter 66) 
types of studies in, (Clinical Volume 5, Chapter 66) 
Resolution acuity, (Clinical Volume 2, Chapter 2) See also Visual acuity, (Foundations Volume 2, Chapter 17) 
Resolving power
diffraction and, (Clinical Volume 1, Chapter 3) 
pupillary diameter and, (Clinical Volume 1, Chapter 33) 
Respiratory acidosis, carbonic anhydrase inhibitors and, (Foundations Volume 3, Chapter 30) 
Respiratory choristoma, (Clinical Volume 4, Chapter 10) 
Respiratory syncytial virus, (Foundations Volume 2, Chapter 85) 
Respiratory system. See also specific respiratory disorders
general anesthesia and, in children, (Clinical Volume 6, Chapter 81) 
Restoration point, fusion, (Clinical Volume 1, Chapter 7) 
Restriction enzymes, (Foundations Volume 1, Chapter 19A) 
in prenatal diagnosis, (Foundations Volume 3, Chapter 56) 
Restriction fragment length polymorphism, (Foundations Volume 1, Chapter 19A) 
Restrictive fragment length polymorphism (RFLP), (Foundations Volume 3, Chapter 55) 
Restrictive syndromes, 32
Brown tendon sheath syndrome, 32–34
congenital fibrosis syndromes, 34–35
Restrictive syndromes, congenital, (Clinical Volume 2, Chapter 13) 
Retained lens material, (Clinical Volume 6, Chapter 65 ) 
Reticuloendotheliosis, benign. See Cat-scratch disease
Reticulohistiocytoma, (Clinical Volume 4, Chapter 10) 
Reticulosis
malignant, midline, (Clinical Volume 2, Chapter 35) 
polymorphic, (Clinical Volume 2, Chapter 35) See also Lymphomatoid granulomatosis
Reticulum cell lymphoma, orbital malignancies and, (Clinical Volume 2, Chapter 5) 
Reticulum cell sarcoma. See Sarcoma, reticulum cell
Reticulum of Muller, (Clinical Volume 4, Chapter 31) 
Retina, (Foundations Volume 2, Chapter 12) (Foundations Volume 3, Chapter 13) 
abiotrophies of, (Clinical Volume 2, Chapter 5) 
ablation of, in ocular ischemic syndrome, (Clinical Volume 3, Chapter 12) 
abnormalities of, amblyopia and, (Clinical Volume 1, Chapter 10) 
alpha-adrenergic drug effects on, (Foundations Volume 3, Chapter 29) 
amacrine cells, (Foundations Volume 1, Chapter 20) See also Amacrine cells
amacrine cells of, (Clinical Volume 3, Chapter 1) 
angioma of, cavernous, (Clinical Volume 2, Chapter 17) 
angiomatosis of. (See Von Hippel-Lindau disease)
anomalous correspondence, (Foundations Volume 2, Chapter 24) 
arterial obstructive disease affecting, fluorescein angiography, (Foundations Volume 2, Chapter 113C ) 
in arterial occlusive disease, (Clinical Volume 2, Chapter 5 ) 
arteriolar narrowing in, in hypertension, 2, (Clinical Volume 3, Chapter 13) 
arteriovenous communications and, (Clinical Volume 3, Chapter 22) 
arteriovenous communication with brain, (Foundations Volume 3, Chapter 2) 
arteriovenous malformation and, (Clinical Volume 3, Chapter 22) 
astrocytic hamartoma
in tuberous sclerosis, (Foundations Volume 3, Chapter 58) 
astrocytoma in, in tuberous sclerosis, (Clinical Volume 3, Chapter 34) 
axonal transport. (See Optic nerve, axonal transport)
in Batten-Mayou syndrome, (Clinical Volume 2, Chapter 5) 
in Berman disease (MLS IV), (Clinical Volume 4, Chapter 14) 
bipolar cells. (See Bipolar cells)
bipolar cells in, (Clinical Volume 3, Chapter 1) 
black sunbursts in, in sickle cell disease, (Clinical Volume 3, Chapter 17) 
blood and, barrier function, (Foundations Volume 2, Chapter 61) 
in blood dyscrasias, (Clinical Volume 3, Chapter 18 ) 
blood vessels of, (Clinical Volume 3, Chapter 1) (Clinical Volume 3, Chapter 26) See also Blood vessels, retinal
breaks in. (See Retina, tears in)
cavernous hemangioma, (Foundations Volume 2, Chapter 113A) 
cell layers of, 3, (Clinical Volume 3, Chapter 1) 
cells, (Foundations Volume 1, Chapter 20) See also specific type
in choroditis
commotio retinae and, (Clinical Volume 3, Chapter 7) 
complications, (Foundations Volume 3, Chapter 6) 
ultrasound biomicroscopy, (Foundations Volume 2, Chapter 106) 
congenital anomalies, (Foundations Volume 3, Chapter 13 ) 
cotton-wool spots. (See Cotton-wool spots)
cotton-wool spots in, (Clinical Volume 3, Chapter 7) See also Cotton–wool spots, retinal
in cranial arteritis, (Clinical Volume 2, Chapter 5) 
cystic disease of, 3–4, (Clinical Volume 3, Chapter 9) 
degenerative disorders of, (Clinical Volume 3, Chapter 26) 
detachment, (Foundations Volume 3, Chapter 13) 
after cataract surgery, (Foundations Volume 3, Chapter 6) 
automated perimetry in, (Foundations Volume 2, Chapter 109) 
from blunt trauma, (Foundations Volume 3, Chapter 6) 
familial exudative vitreoretinopathy and, (Foundations Volume 3, Chapter 61) 
indirect-acting muscarinic agonists and, (Foundations Volume 3, Chapter 26) 
optical coherence tomography, (Foundations Volume 2, Chapter 107) 
pathologic changes following, (Foundations Volume 3, Chapter 13) 
and postoperative color Doppler imaging after, (Foundations Volume 2, Chapter 102) 
predisposing conditions, (Foundations Volume 3, Chapter 13) 
recurrent traction, (Foundations Volume 3, Chapter 18) 
retinoblastoma versus, (Foundations Volume 3, Chapter 21) 
retinoschisis versus, (Foundations Volume 2, Chapter 107) 
detachment of. (See Retinal detachment)
developmental malformations of, (Clinical Volume 3, Chapter 26) 
diabetes. (See Retinopathy, diabeticin)
in diabetes mellitus, (Foundations Volume 3, Chapter 18 ) 
diseases
automated perimetry and, (Foundations Volume 2, Chapter 109) 
clinical assessment, (Foundations Volume 2, Chapter 14) 
Epstein-Barr virus and, (Foundations Volume 2, Chapter 91) 
fluorescein angiography in, (Foundations Volume 2, Chapter 113) 
inherited with known molecular defect, (Foundations Volume 1, Chapter 19A) 
disorders of, (Clinical Volume 2, Chapter 5 ) 
genetic approaches to, (Clinical Volume 3, Chapter 2) 
molecular pathogenesis of, (Clinical Volume 3, Chapter 2) 
monocular, temporal profile of, (Clinical Volume 2, Chapter 5) 
disruption, posterior vitreous detachment and, (Foundations Volume 1, Chapter 16) 
early differentiation in, (Foundations Volume 1, Chapter 2) 
edema of. (See also Edema, retinal)
electroretinogram of. (See Electroretinography (ERG))
enclosed ora bay in, (Clinical Volume 3, Chapter 26) 
in ethylmalonic aciduria, (Clinical Volume 5, Chapter 19) 
external limiting membrane of, (Foundations Volume 1, Chapter 19) 
exudates of. (See Cotton-wool spots, retinal; Exudates, retinal)
fiber layer of Henle in, (Clinical Volume 3, Chapter 1) 
fishtail lesions in, (Clinical Volume 3, Chapter 9) 
fluorescein angiography of, (Foundations Volume 2, Chapter 113) 
abnormal vessels in, (Clinical Volume 4, Chapter 57) 
blocked fluorescence in, 2, (Clinical Volume 4, Chapter 57) 
vascular filling defect in, 3, (Clinical Volume 4, Chapter 57) 
formation of layers, (Foundations Volume 1, Chapter 2) 
fovea. (See Fovea)
fovea of. (See Fovea, retinal)
function of, (Clinical Volume 3, Chapter 2 ) 
electrophysiologic tests of, (Clinical Volume 3, Chapter 2) 
neurocircuitry of, (Clinical Volume 3, Chapter 3) 
photoreceptors in, (Clinical Volume 3, Chapter 2) 
ganglion cell layer of, (Foundations Volume 1, Chapter 1) 
ganglion cells. (See Ganglion cells, retinal)
gastrointestinal disorders involving, (Clinical Volume 5, Chapter 30) 
generalized diseases of, (Clinical Volume 3, Chapter 26) 
in glycogen storage disease, (Clinical Volume 5, Chapter 30) 
gyrate atrophy of. (See Gyrate atrophy)
in hamartoma syndromes, (Clinical Volume 2, Chapter 5) 
hemangioblastoma of, in von Hippel-Lindau disease, (Clinical Volume 3, Chapter 34) 
hemangioma of
capillary, (Clinical Volume 3, Chapter 22) 
photocoagulation of, (Clinical Volume 6, Chapter 76) 
in von Hippel-Lindau disease, (Clinical Volume 3, Chapter 34) 
hemorrhagic infarction, (Foundations Volume 3, Chapter 13) 
hemorrhaging in, 3, (Clinical Volume 3, Chapter 30) 
cytomegalovirus and, (Clinical Volume 3, Chapter 7) 
malignant hypertension and, 2, (Clinical Volume 5, Chapter 31) 
ocular ischemic syndrome and, (Clinical Volume 3, Chapter 12) 
ophthalmoscopy in, (Clinical Volume 3, Chapter 7) 
pregnancy-induced hypertension and, (Clinical Volume 5, Chapter 32) 
sickle cell disease and, (Clinical Volume 3, Chapter 17) 
heredodegenerative disorders of, (Clinical Volume 2, Chapter 5) 
molecular genetics of, (Clinical Volume 3, Chapter 2 ) 
in herpes zoster ophthalmicus, (Clinical Volume 4, Chapter 20) 
horizontal cells, (Foundations Volume 1, Chapter 20) See also Horizontal cells
image sizes on, (Clinical Volume 1, Chapter 33) 
in anisometropia, (Clinical Volume 1, Chapter 33) 
in axial hyperopia, after spectacle correction, (Clinical Volume 1, Chapter 33) 
in axial myopia, after spectacle correction, (Clinical Volume 1, Chapter 33) 
spectacle magnification and, (Clinical Volume 1, Chapter 33 ) 
indirect-acting muscarinic agonists and, (Foundations Volume 3, Chapter 26) 
infectious disease and, (Clinical Volume 3, Chapter 26) 
inflammatory cells in, (Clinical Volume 3, Chapter 7) 
inner limiting membrane of, (Foundations Volume 1, Chapter 1) 
inner nuclear layer of, (Foundations Volume 1, Chapter 19) 
inner plexiform layer. (See Inner plexiform layer (IPL))
inner plexiform layer of, (Foundations Volume 1, Chapter 19) 
intercellular spaces, (Foundations Volume 1, Chapter 19) 
interference fringes on, (Clinical Volume 1, Chapter 66) See also Laser(s)
internal limiting membrane, (Foundations Volume 1, Chapter 16) (Foundations Volume 1, Chapter 19) 
posterior vitreous detachment and, (Foundations Volume 1, Chapter 16) 
internal limiting membrane of, (Foundations Volume 1, Chapter 19) 
interphotoreceptor matrix in, (Clinical Volume 3, Chapter 1) 
interplexiform cells, (Foundations Volume 1, Chapter 20) 
interplexiform cells in, (Clinical Volume 3, Chapter 1) 
iridescent spots in, in sickle cell disease, (Clinical Volume 3, Chapter 17) 
kidney disease, (Clinical Volume 5, Chapter 31) See also Kidney diseasein
light scattering in, (Clinical Volume 1, Chapter 31) 
light toxicity in
from operating microscope, following IOL implantation, (Clinical Volume 1, Chapter 68) 
limiting membrane of
lipid accumulation in, 2, (Clinical Volume 3, Chapter 7) 
macroaneurysms, (Foundations Volume 3, Chapter 13) 
fluorescein angiography, (Foundations Volume 2, Chapter 113C) 
macula. (See Macula)
macula of, (Clinical Volume 3, Chapter 1) See Macula
mechanical interfacial separation of vitreous from, (Foundations Volume 2, Chapter 11) 
meridional complex of, (Clinical Volume 3, Chapter 26) 
with peripheral retinal excavation, (Clinical Volume 3, Chapter 26) 
meridional fold in, (Clinical Volume 3, Chapter 26) 
metastatic cancer to, (Clinical Volume 5, Chapter 34) 
microemboli of, (Clinical Volume 2, Chapter 5) 
in carotid artery disease, (Clinical Volume 3, Chapter 14) 
microglial distribution in, (Foundations Volume 1, Chapter 19) 
microvascular abnormalities, (Foundations Volume 3, Chapter 18) 
molecular biology and genetics, (Foundations Volume 1, Chapter 19A) 
molecular physiology and pathology of, (Clinical Volume 3, Chapter 2 ) 
in Morquio syndrome, (Foundations Volume 3, Chapter 54B) 
in mucopolysaccharidoses, (Clinical Volume 5, Chapter 30) 
myelinated nerve fibers in, (Clinical Volume 3, Chapter 8) 
necrosis
fluorescein angiography of, (Foundations Volume 2, Chapter 113E) 
toxoplasmic, in AIDS, (Foundations Volume 2, Chapter 82) 
necrosis of, (Clinical Volume 3, Chapter 7) See also Retinal necrosis syndrome, acute (ARN)
outer, progressive, (Clinical Volume 4, Chapter 37) See also Progressive outer retinal necrosis syndrome (PORN)
neovascularization
in diabetes mellitus, (Foundations Volume 3, Chapter 18) 
in peripheral proliferative retinopathies, (Foundations Volume 2, Chapter 113C) 
vitreous hemorrhage and, (Foundations Volume 3, Chapter 14) 
neovascular proliferation of. (See Neovascularization)
neuroglia. (See Glial cells, retinal)
neuromodulatory systems, (Foundations Volume 1, Chapter 20) 
neuro-ophthalmologic examination, (Clinical Volume 2, Chapter 10) 
ganglion cells, on/off dichotomy, (Clinical Volume 2, Chapter 10) 
parallel visual pathways, (Clinical Volume 2, Chapter 10) 
magnocellular, parvocellular parallel pathway, (Clinical Volume 2, Chapter 10) 
receptive fields, (Clinical Volume 2, Chapter 10) 
retino-cortical visual pathway, (Clinical Volume 2, Chapter 10) 
normal, optic nerve and, (Clinical Volume 3, Chapter 48) 
opacification of, gray-white, (Clinical Volume 3, Chapter 7) 
optical coherence tomography, (Foundations Volume 2, Chapter 107 ) 
optical coherence tomography of, (Clinical Volume 1, Chapter 48A) 
ora serrata. (See Ora serrata)
outer, information processing, (Foundations Volume 1, Chapter 20) 
outer nuclear layer of, (Foundations Volume 1, Chapter 19) 
outer plexiform layer. (See Outer plexiform layer (OPL))
outer plexiform layer of, (Foundations Volume 1, Chapter 19) 
output pathway to brain, (Foundations Volume 2, Chapter 13) 
oxygen saturation, (Foundations Volume 2, Chapter 5) 
in pathologic myopia, (Clinical Volume 3, Chapter 36) 
perforation of, in surgery for strabismus, (Clinical Volume 4, Chapter 62) 
perifovea. (See Perifovea)
perimacular deposits on
in glycogen storage diseases, (Clinical Volume 5, Chapter 30) 
in sphingolipidoses, (Clinical Volume 5, Chapter 30) 
peripheral, (Foundations Volume 1, Chapter 1) 
age-related changes in, (Clinical Volume 3, Chapter 26) 
cryotherapy of, in diabetic retinopathy, (Clinical Volume 3, Chapter 30) 
degenerative diseases of, (Clinical Volume 3, Chapter 26 ) 
developmental variations in, (Clinical Volume 3, Chapter 26) 
ophthalmoscopy of, (Clinical Volume 3, Chapter 7) 
in sickle cell disease, (Clinical Volume 3, Chapter 17) 
peripheral albinotic spots, (Foundations Volume 3, Chapter 13) 
periphery
in peroxisomal disorders, (Clinical Volume 5, Chapter 30) 
pharmacokinetics and, (Foundations Volume 3, Chapter 23) 
photochemistry, (Foundations Volume 2, Chapter 12) See also Photoreceptor(s)
photocoagulation of, (Clinical Volume 6, Chapter 76) See also Photocoagulation
photoreceptor cells. (See Photoreceptor(s))
photoreceptors in. (See Photoreceptors, retinal)
pigmentary abnormalities in
in progressive external ophthalmoplegia, (Clinical Volume 2, Chapter 12) 
in tuberous sclerosis, (Clinical Volume 5, Chapter 36) 
pigmentary degeneration of, cataracts and, (Clinical Volume 5, Chapter 41) 
pigmentary degeneration of, syndromes including, (Clinical Volume 5, Chapter 41) 
pigment epithelium. (See Retinal pigment epithelium (RPE))
preretinal vascular loops in, (Clinical Volume 3, Chapter 8) 
Purtscher’s retinopathy and, (Clinical Volume 3, Chapter 32) 
relative afferent pupillary defect and, (Clinical Volume 2, Chapter 15) 
retinitis pigmentosa and. (See Retinitis pigmentosa)
in retrolental fibroplasia. (See Retinopathy of prematurity (retrolental fibroplasia))
rods and cones of, (Clinical Volume 3, Chapter 1) See also under Photoreceptors
Sandhoff disease and, (Foundations Volume 3, Chapter 54B) 
sequelae of nongranulomatous inflammation, (Foundations Volume 3, Chapter 3) 
sickle cell retinopathy and. (See Sickle cell disease)
spatial processing, (Foundations Volume 2, Chapter 13) 
in sphingolipidoses, (Clinical Volume 5, Chapter 30) 
storage and transport, (Foundations Volume 2, Chapter 12) 
synaptic connections in, (Clinical Volume 3, Chapter 1) 
systemic diseases involving, (Foundations Volume 3, Chapter 13) 
Tay-Sachs disease and, (Foundations Volume 3, Chapter 54B) 
tears of, (Clinical Volume 3, Chapter 26) 
in acute retinal necrosis syndrome, (Clinical Volume 3, Chapter 28) 
iatrogenic, diabetic vitrectomy and, (Clinical Volume 6, Chapter 57) 
localization of, for scleral buckling, (Clinical Volume 6, Chapter 59) 
ophthalmoscopy of, 2, (Clinical Volume 3, Chapter 7) 
partial-thickness, (Clinical Volume 3, Chapter 2) 
in pathologic myopia, (Clinical Volume 3, Chapter 36) 
surgical anatomy of, (Clinical Volume 6, Chapter 51) 
in venous obstructive disease, (Clinical Volume 3, Chapter 15 ) 
vitrectomy-related, (Clinical Volume 6, Chapter 56) 
vitreous base of, (Clinical Volume 3, Chapter 26) 
vitreous traction, (Clinical Volume 3, Chapter 31) 
telangiectasis of, (Clinical Volume 3, Chapter 22) 
photocoagulation in, (Clinical Volume 6, Chapter 76) 
topical drugs and, (Clinical Volume 3, Chapter 57) 
toxic effects of light on, (Foundations Volume 2, Chapter 15) 
in toxoplasmosis, (Clinical Volume 4, Chapter 46) 
traumatic disorders of, (Clinical Volume 3, Chapter 26) 
trauma to, distant extraocular trauma and, (Clinical Volume 3, Chapter 32 ) 
ultrasonography of, (Clinical Volume 3, Chapter 3 ) 
vascular disorders of, (Clinical Volume 3, Chapter 26) 
vascular system, (Foundations Volume 2, Chapter 5) See also Retinal artery; Retinal veins
arterial obstructive disease affecting, fluorescein angiography, (Foundations Volume 2, Chapter 113C ) 
in diabetes mellitus, (Foundations Volume 3, Chapter 18) 
dystrophies, fluorescein angiography
vitreoretinal interface and, (Foundations Volume 1, Chapter 16) 
vasculature of
visual function testing, (Foundations Volume 2, Chapter 14 ) 
vitrectomy complications of
vitreous interface of, (Clinical Volume 6, Chapter 51) 
vitreous interface with, (Foundations Volume 1, Chapter 16) 
ultrasound evaluation, (Foundations Volume 2, Chapter 108) 
vitreous separation from, (Foundations Volume 2, Chapter 11) 
in von Gierke’s disease, (Clinical Volume 5, Chapter 30) 
in von Hippel-Lindau disease, (Foundations Volume 3, Chapter 58) 
wavelength of light and, (Foundations Volume 2, Chapter 15) 
“white-without-pressure, ”, (3) 7: 22
“white-with-pressure, ”, (3) 7: 22
Retinaculum, lateral, (Foundations Volume 1, Chapter 5) 
Retinal and retinal pigment epithelium detachment, (Clinical Volume 3, Chapter 18) 
Retinal arterial macroaneurysm, fluorescein angiography, (Foundations Volume 2, Chapter 113C) 
Retinal arterial obstructive disease, (Foundations Volume 2, Chapter 113C) 
Retinal arteries
central, (Clinical Volume 2, Chapter 4) 
in central retinal vein obstruction, (Clinical Volume 3, Chapter 15) 
occlusion of, (Clinical Volume 3, Chapter 7) (Clinical Volume 3, Chapter 14) 
after keratomileusis, (Clinical Volume 6, Chapter 46) 
with cilioretinal artery sparing, (Clinical Volume 3, Chapter 14) 
in hypertensive retinopathy, (Clinical Volume 3, Chapter 13) 
in sickle cell disease, (Clinical Volume 3, Chapter 17) 
hereditary tortuosity of, (Clinical Volume 3, Chapter 22) 
macroaneurysms of, in hypertensive retinopathy, (Clinical Volume 3, Chapter 13) 
necrosis of
platelet abnormalities and, (Clinical Volume 5, Chapter 23) 
in protein S deficiency, (Clinical Volume 5, Chapter 23) 
ocular ischemic syndrome and, (Clinical Volume 3, Chapter 12) 
Retinal arterioles. See Arterioles, retinal
Retinal artery obstruction, (Clinical Volume 3, Chapter 14) 
with cilioretinal artery sparing, (Clinical Volume 3, Chapter 14) 
Retinal artery occlusion, (Clinical Volume 5, Chapter 32) 
Retinal blur, vergence triggered by, (Clinical Volume 1, Chapter 4) 
Retinal capillary hemangioma, (Foundations Volume 3, Chapter 20) 
Retinal changes with pregnancy, (Clinical Volume 5, Chapter 32) 
Retinal correspondence, (Clinical Volume 1, Chapter 5) (Clinical Volume 1, Chapter 8) 
afterimage test of, (Clinical Volume 1, Chapter 9) 
anomalous, treatment of, (Clinical Volume 1, Chapter 9) 
Bagolini striated glasses test of, (Clinical Volume 1, Chapter 9) 
Lancaster projectors in studies of, (Clinical Volume 1, Chapter 9) 
major amblyoscope test of, (Clinical Volume 1, Chapter 9) 
red filter test of, (Clinical Volume 1, Chapter 9) 
Retinal depression sign, in sickle cell disease, (Clinical Volume 3, Chapter 17) 
Retinal detachment, (Clinical Volume 3, Chapter 31) (Clinical Volume 3, Chapter 55) (Clinical Volume 4, Chapter 45) 
in acute retinal necrosis syndrome, (Clinical Volume 3, Chapter 28) 
after vitrectomy, (Clinical Volume 6, Chapter 56) 
anesthesia-related, (Clinical Volume 6, Chapter 1) 
angioid streaks and, (Clinical Volume 3, Chapter 36) 
aphakic, vitrectomy for, (Clinical Volume 6, Chapter 56) 
branch retinal vein occlusion and, (Clinical Volume 3, Chapter 15) 
from cataract surgery, (Clinical Volume 3, Chapter 55) 
chemodenervation in, (Clinical Volume 6, Chapter 89) 
ciliochoroidal effusion versus, (Clinical Volume 4, Chapter 52) 
cytomegalovirus and, (Clinical Volume 3, Chapter 28A) 
in disseminated intravascular coagulation, (Clinical Volume 5, Chapter 23) 
exudative
in cytomegalovirus retinitis, (Clinical Volume 3, Chapter 28A) 
in kidney disease, 2, (Clinical Volume 5, Chapter 31) 
postoperative, (Clinical Volume 5, Chapter 16) 
after scleral buckling, (Clinical Volume 6, Chapter 59) 
with giant retinal tears, vitrectomy for, (Clinical Volume 6, Chapter 56) 
in kidney disease, (Clinical Volume 5, Chapter 31) 
lens fragments and, (Clinical Volume 6, Chapter 65) 
with media opacities, vitrectomy for, (Clinical Volume 6, Chapter 56) 
Nd:YAG laser posterior capsulotomy and, (Clinical Volume 6, Chapter 10) 
in papillorenal syndrome, (Clinical Volume 5, Chapter 31) 
in pars planitis, (Clinical Volume 4, Chapter 43) 
in pathologic myopia, (Clinical Volume 3, Chapter 36) 
pediatric
after cataract surgery, (Clinical Volume 6, Chapter 100) 
surgical management of, (Clinical Volume 6, Chapter 72 ) 
in Pierre Robin syndrome, (Clinical Volume 5, Chapter 29) 
with posterior breaks, vitrectomy for, (Clinical Volume 6, Chapter 56) 
in progressive outer retinal necrosis syndrome, (Clinical Volume 3, Chapter 28) 
with proliferative vitreoretinopathy, (Clinical Volume 6, Chapter 56) See also Vitreoretinopathy, 13–14, 17–18, 26–27; (Clinical Volume 6, Chapter 58) 
pseudophakic. (See also Pseudophakia)
scleral buckling in, (Clinical Volume 6, Chapter 59) 
recurrent, after vitreous surgery, for proliferative vitreoretinopathy, (Clinical Volume 6, Chapter 58) 
in retinopathy of prematurity, surgical management of, (Clinical Volume 6, Chapter 56) (Clinical Volume 6, Chapter 72) 
rhegmatogenous, (Clinical Volume 3, Chapter 26) (Clinical Volume 3, Chapter 27)  (Clinical Volume 3, Chapter 30) (Clinical Volume 3, Chapter 39) 
in cytomegalovirus retinitis, (Clinical Volume 3, Chapter 28A) 
proliferative vitreoretinopathy in. (See Vitreoretinopathy, proliferative)
scleral buckling in, (Clinical Volume 6, Chapter 72) 
traction and, vitrectomy in, (Clinical Volume 6, Chapter 57) 
secondary IOL implantation and, (Clinical Volume 6, Chapter 8) 
secondaty to schisis, (Clinical Volume 6, Chapter 76) 
serous, (Clinical Volume 3, Chapter 31) 
in choroidal obstruction, (Clinical Volume 3, Chapter 14) 
in hypertension, (Clinical Volume 3, Chapter 13) 
pregnancy-induced, (Clinical Volume 5, Chapter 32) 
in kidney failure, (Clinical Volume 5, Chapter 31) 
photocoagulation for, (Clinical Volume 6, Chapter 76) 
in sickle cell disease, (Clinical Volume 3, Chapter 17) 
subclinical, photocoagulation for, (Clinical Volume 6, Chapter 76) 
surgery for
anatomic considerations on, (Clinical Volume 6, Chapter 51) 
ciliochoroidal effusions from, (Clinical Volume 4, Chapter 63) 
long term tamponade in, (Clinical Volume 6, Chapter 54) 
proliferative vitreoretinopathy and. (See Vitreoretinopathy, proliferative)
scleral buckling as. (See Scleral buckling surgery)
in sickle cell retinopathy, (Clinical Volume 3, Chapter 17) 
ultrasonography in, (Clinical Volume 3, Chapter 3) 
viral retinitis-related, (Clinical Volume 6, Chapter 56) 
vitreoretinal adhesions and, (Clinical Volume 6, Chapter 56) 
Retinal diagnostic testing in pregnancy, (Clinical Volume 5, Chapter 32) 
fluorescein angiography, (Clinical Volume 5, Chapter 32) 
indocyanine green angiography, (Clinical Volume 5, Chapter 32) 
Retinal disc neovascularization, (Clinical Volume 3, Chapter 18) 
Retinal disorders in pregnancy, (Clinical Volume 5, Chapter 32) 
Retinal disparity, vergence triggered by, (Clinical Volume 1, Chapter 4) 
Retinal eccentricity, (Foundations Volume 2, Chapter 24) 
Retinal folds, falciform, (Foundations Volume 3, Chapter 53) 
Retinal ganglion cell axons, optic nerve and, (Foundations Volume 2, Chapter 21) 
Retinal hemorrhage, (Clinical Volume 3, Chapter 31) 
Retinal hemorrhages, (Clinical Volume 3, Chapter 18) 
in shaken baby syndrome, (Clinical Volume 5, Chapter 44) 
Retinal image similarity versus dissimilarity in strabismus, (Clinical Volume 1, Chapter 8) 
Retinal imaging, wavefront technology and, (Clinical Volume 1, Chapter 70) 
Retinal infiltrates, (Clinical Volume 3, Chapter 18) 
Retinal macropsia, (Clinical Volume 2, Chapter 7) 
Retinal manifestations with gastrointestinal disease, (Clinical Volume 5, Chapter 30) 
Retinal metamorphopsia, (Clinical Volume 2, Chapter 7) 
Retinal micropsia, (Clinical Volume 2, Chapter 7) 
Retinal necrosis syndrome
acute, acyclovirin in, (Foundations Volume 3, Chapter 37) 
acute (ARN), (Clinical Volume 3, Chapter 28)  (Clinical Volume 4, Chapter 44) (Clinical Volume 4, Chapter 45)  (Clinical Volume 4, Chapter 57) 
bilateral involvement in, (Clinical Volume 3, Chapter 28) 
clinical presentation of, (Clinical Volume 3, Chapter 28) 
cytomegalovirus retinitis versus, (Clinical Volume 3, Chapter 28A) 
diagnostic evaluation and ancillary tests for, (Clinical Volume 3, Chapter 28) 
differential diagnosis of, (Clinical Volume 3, Chapter 28) 
etiology and histopathology of, (Clinical Volume 3, Chapter 28) 
historical perspective on, (Clinical Volume 3, Chapter 28) 
in immunocompromised patients, (Clinical Volume 3, Chapter 28) 
platelet abnormalities and, (Clinical Volume 5, Chapter 23) 
treatment of, (Clinical Volume 3, Chapter 28) 
retinal detachment and, (Clinical Volume 3, Chapter 28) 
Retinal-neuro-cutaneous cavernous hemangioma syndrome, (Clinical Volume 3, Chapter 34) 
Retinal organization, (Clinical Volume 3, Chapter 6) 
Retinal pigmentary dystrophy, (Clinical Volume 2, Chapter 5) 
Retinal pigment epitheliopathy, drug-induced
Retinal pigment epithelitis, (Clinical Volume 4, Chapter 49) 
Retinal pigment epithelium, congenital hypertrophy of, in familial adenomatous polyposis coli, (Clinical Volume 5, Chapter 30) 
Retinal pigment epithelium (RPE), (Foundations Volume 1, Chapter 21)  (Foundations Volume 2, Chapter 13) (Clinical Volume 3, Chapter 1) (Clinical Volume 4, Chapter 31) 
in acute retinal necrosis syndrome, (Clinical Volume 3, Chapter 28) 
age-related macular degeneration, (Foundations Volume 1, Chapter 21) 
angioid streaks and, (Clinical Volume 3, Chapter 36) 
apical membrane specializations, (Foundations Volume 1, Chapter 21) 
atrophy of, in choroideremia, (Clinical Volume 3, Chapter 25A) 
in autosomal dominant fundus flavimaculatus, (Clinical Volume 3, Chapter 9) 
basal lamina of, (Clinical Volume 3, Chapter 1) 
in benign concentric annular macular dystrophy, (Clinical Volume 3, Chapter 9) 
blood-retinal barrier and, (Foundations Volume 1, Chapter 21) 
Bruch’s membrane and, (Foundations Volume 1, Chapter 21) 
in butterfly-shaped pigment dystrophy of fovea, (Clinical Volume 3, Chapter 9) 
in central areolar pigment epithelial dystrophy, (Clinical Volume 3, Chapter 9) 
in central serous chorioretinopathy, (Clinical Volume 3, Chapter 4A) 
characteristics of, (Foundations Volume 1, Chapter 21) 
congenital abnormalities of, (Clinical Volume 3, Chapter 8) 
congenital disorders of, (Foundations Volume 1, Chapter 21) 
congenital hypertrophy of, (Clinical Volume 5, Chapter 30) 
degeneration of. (See Retinitis pigmentosa)
detachment
fibrovascular, optical coherence tomography, (Foundations Volume 2, Chapter 107) 
hemorrhagic, optical coherence tomography, (Foundations Volume 2, Chapter 107) 
differentiation of, (Foundations Volume 1, Chapter 21) 
in dominant cystoid macular dystrophy, (Clinical Volume 3, Chapter 9) 
in dominant slowly progressive macular dystrophy, (Clinical Volume 3, Chapter 9) 
embryonic development of, (Foundations Volume 1, Chapter 21) 
epitheliitis of, (Clinical Volume 4, Chapter 37) (Clinical Volume 4, Chapter 57) See also Epitheliitis, retinal pigment
experimental models of, (Foundations Volume 1, Chapter 21) 
in familial adenomatous polyposis coli, (Clinical Volume 5, Chapter 30) 
in familial drusen, (Clinical Volume 3, Chapter 9) 
in fenestrated sheen macular dystrophy, (Clinical Volume 3, Chapter 9) 
in foveomacular vitelliform dystrophy, (Clinical Volume 3, Chapter 9) 
in fundus flavimaculatus, (Clinical Volume 3, Chapter 9) 
ganglion cells of, (Clinical Volume 3, Chapter 1) 
genetic engineering of, (Foundations Volume 1, Chapter 21) 
genomic analysis of, (Foundations Volume 1, Chapter 21) 
hereditary macular dystrophies involving, (Clinical Volume 3, Chapter 9 ) 
histologic features of, (Foundations Volume 1, Chapter 21) 
interphotoreceptor matrix, (Foundations Volume 1, Chapter 21) 
interphotoreceptor retinoid binding protein, (Foundations Volume 1, Chapter 21) 
ion channels in, (Clinical Volume 3, Chapter 1) 
lateral surface of, (Foundations Volume 1, Chapter 21) 
lipofuscin granules in, (Clinical Volume 3, Chapter 1) 
macroreticular dystrophy of, (Clinical Volume 3, Chapter 9) 
melanin granules in, (Clinical Volume 3, Chapter 1) 
membrane discs of, (Clinical Volume 3, Chapter 1) 
in membranoproliferative glomerulonephritis, (Clinical Volume 5, Chapter 31) 
morphological organization of, (Foundations Volume 1, Chapter 1) 
nuclear layers of, (Clinical Volume 3, Chapter 1) 
in patholgic myopia, (Clinical Volume 3, Chapter 36) 
pattern dystrophy of, (Clinical Volume 3, Chapter 9) 
in pericentral rod-cone dystrophy, (Clinical Volume 3, Chapter 9) 
in photoreceptor outer segment phagocytosis, (Foundations Volume 1, Chapter 21) 
in physiologic myopia, (Clinical Volume 3, Chapter 36) 
plasma membrane of, (Clinical Volume 3, Chapter 1) 
potentials, (Foundations Volume 2, Chapter 13) See also Electro–oculogram (EOG)
in progressive cone-rod dystrophies, (Clinical Volume 3, Chapter 9) 
proliferative vitreoretinopathy, (Foundations Volume 1, Chapter 21) 
proteomic analysis of, (Foundations Volume 1, Chapter 21) 
retinoid processing and, (Foundations Volume 1, Chapter 21) 
with rod monochromaticism, (Clinical Volume 3, Chapter 9) 
“salt and pepper” appearance of, in cytomegalovirus retinitis, (Clinical Volume 3, Chapter 28A) 
scar formation in, (Clinical Volume 3, Chapter 7) 
Sjorgren’s reticular dystrophy of, (Clinical Volume 3, Chapter 9) 
specialization of
in Stargardt’s disease, (Clinical Volume 3, Chapter 9) 
subfoveal membranes anterior to, surgical removal of, (Clinical Volume 6, Chapter 62) 
synapses, embryology, (Foundations Volume 1, Chapter 2) 
toxoplasmic invasion, in AIDS, (Foundations Volume 2, Chapter 82) 
transplantation of, (Foundations Volume 1, Chapter 21) 
uveal melanocytes versus, (Foundations Volume 3, Chapter 20) 
uveal melanoma and, (Foundations Volume 3, Chapter 20) 
window defect in, (Clinical Volume 4, Chapter 57) 
Retinal ray tracing technique, of aberration measurement, (Clinical Volume 1, Chapter 70) 
Retinal reattachment surgery
Retinal rivalry, (Clinical Volume 1, Chapter 5) 
Retinal tears, (Clinical Volume 3, Chapter 31) 
cryotherapy treatment for, (Clinical Volume 6, Chapter 60) 
laser treatment for, (Clinical Volume 6, Chapter 60) 
role of head trauma in, (Clinical Volume 3, Chapter 31) 
vitreous traction tears, (Clinical Volume 3, Chapter 31) 
Retinal vascular changes, (Clinical Volume 3, Chapter 18) 
Retinal vascular diseases, fluorescein angiography for, (Foundations Volume 2, Chapter 113C ) 
Retinal vasculitis
in acute retinal necrosis syndrome, 3, (Clinical Volume 3, Chapter 28) 
in cytomegalovirus retinitis, (Clinical Volume 3, Chapter 28A) 
Eales’ disease. (See Eales’ diseasein)
fluorescein angiography of, (Clinical Volume 4, Chapter 57) 
in gastrointestinal disorders, (Clinical Volume 5, Chapter 30) 
idiopathic, syndrome of aneurysms and neuroretinitis and, (Clinical Volume 3, Chapter 22) 
Retinal vein occlusion, (Clinical Volume 5, Chapter 32) 
Retinal veins, (Foundations Volume 1, Chapter 19) (Foundations Volume 2, Chapter 5) 
beading of
in diabetic retinopathy, (Clinical Volume 3, Chapter 30) 
central, (Foundations Volume 2, Chapter 5) 
occlusion
color Doppler imaging, (Foundations Volume 2, Chapter 102) 
fluorescein angiography, (Foundations Volume 2, Chapter 113C) 
oscillatory potentials, (Foundations Volume 2, Chapter 14) 
loops in, in diabetic retinopathy, (Clinical Volume 3, Chapter 30) 
obstruction of, (Clinical Volume 2, Chapter 5) (Clinical Volume 3, Chapter 7) (Clinical Volume 3, Chapter 15 ) 
central, (Clinical Volume 3, Chapter 15)  (Clinical Volume 5, Chapter 23) See also Retinal vasculitis
angle-closure glaucoma versus, (Clinical Volume 3, Chapter 53) 
carotid artery stenosis and, (Clinical Volume 3, Chapter 15) 
central retinal artery occlusion and, (Clinical Volume 3, Chapter 14) (Clinical Volume 3, Chapter 15) 
classification of, (Clinical Volume 3, Chapter 15) 
clinical characteristics of, (Clinical Volume 3, Chapter 15) 
complications of, (Clinical Volume 3, Chapter 15) 
in contralateral eye, (Clinical Volume 3, Chapter 15) 
disorders associated with, (Clinical Volume 3, Chapter 15) 
fluorescein angiography in, (Clinical Volume 3, Chapter 15) 
neovascularization in, (Clinical Volume 3, Chapter 15) 
ophthalmoscopy in, (Clinical Volume 3, Chapter 15) 
papillophlebitis and, (Clinical Volume 3, Chapter 15) 
in sickle cell disease, (Clinical Volume 3, Chapter 17) 
occlusion, in AIDS, (Foundations Volume 2, Chapter 36) 
in ocular ischemic syndrome, (Clinical Volume 3, Chapter 12) 
periphlebitis retinae and, (Clinical Volume 3, Chapter 16 ) 
sheathing, Eales’ disease and, 2, (Clinical Volume 3, Chapter 16) 
tortuosity of, in sickle cell disease, (Clinical Volume 3, Chapter 17) 
Retinal venous obstructive disease, (Foundations Volume 2, Chapter 113C) 
Retinal vitamin A deficiency, hepatobiliary, pancreatic, intestinal diseases, (Clinical Volume 5, Chapter 30) 
Retinectomy, in vitrectomy, (Clinical Volume 6, Chapter 56) 
Retinitis, (Foundations Volume 2, Chapter 40B) (Clinical Volume 4, Chapter 45) 
foveomacular, (Clinical Volume 3, Chapter 37) 
retinal detachment in, (Clinical Volume 6, Chapter 56) 
toxoplasmic retinochoroiditis versus, (Clinical Volume 4, Chapter 46) 
herpes simplex virus, (Clinical Volume 4, Chapter 45) 
herpes zoster, retinal detachment in, (Clinical Volume 6, Chapter 56) 
in immunosuppressed patients, (Clinical Volume 4, Chapter 45 ) 
infectious, (Clinical Volume 4, Chapter 45) See also Infectious retinitis
surgical approaches to, (Clinical Volume 4, Chapter 45 ) 
syphilitic
toxoplasmosis
in Wegener’s granulomatosis, (Clinical Volume 2, Chapter 35) 
Retinitis pigmentosa, (Clinical Volume 2, Chapter 5) (Clinical Volume 3, Chapter 2) (Clinical Volume 3, Chapter 7) (Clinical Volume 3, Chapter 9) (Clinical Volume 3, Chapter 55) (Clinical Volume 3, Chapter 24)  (Clinical Volume 3, Chapter 39) (Foundations Volume 2, Chapter 16) (Foundations Volume 3, Chapter 13) 
autosomal dominant
candidate genes in, (Clinical Volume 3, Chapter 2) 
comparative mapping of, (Clinical Volume 3, Chapter 2) 
molecular genetics, (Foundations Volume 3, Chapter 55) 
not caused by opsin mutation, (Foundations Volume 1, Chapter 19A) 
autosomal recessive
candidate genes in, (Clinical Volume 3, Chapter 2) 
comparative mapping of, (Clinical Volume 3, Chapter 2) 
in Bassen-Kornzweig syndrome, (Clinical Volume 5, Chapter 19) 
choroidal atrophy in, (Clinical Volume 4, Chapter 66) 
dark adaptation in, (Foundations Volume 2, Chapter 14) 
fluorescein angiography, 2, (Foundations Volume 2, Chapter 113B) 
in NARP syndrome, (Clinical Volume 3, Chapter 2) 
in nephronophthisis-associated disorders, (Clinical Volume 5, Chapter 31) 
platelet abnormalities in, (Clinical Volume 5, Chapter 23) 
pseudoretinitis pigmentosa and, (Clinical Volume 3, Chapter 24 ) 
solar damage and, (Clinical Volume 5, Chapter 55) 
thrombocytopenia in, (Clinical Volume 5, Chapter 23) 
Retinitis pigmentosa inversa, (Clinical Volume 2, Chapter 5) 
Retinitis sclopeteria, (Clinical Volume 3, Chapter 31) 
Retinoblastoma, (Clinical Volume 2, Chapter 24) (Clinical Volume 4, Chapter 53) (Foundations Volume 3, Chapter 21 ) 
acute retinal necrosis syndrome versus, (Clinical Volume 3, Chapter 28) 
bilateral, asynchronous, (Clinical Volume 6, Chapter 75) 
clinical management of, (Clinical Volume 6, Chapter 75) 
clinical presentation, 2–3, (Foundations Volume 3, Chapter 21) 
cryotherapy of
differential diagnosis, (Foundations Volume 3, Chapter 21) 
diffuse infiltrating, (Foundations Volume 3, Chapter 21) 
enucleation for
handling of globe after, 5, (Clinical Volume 6, Chapter 109) 
fluorescein angiography, (Foundations Volume 2, Chapter 113A) 
genetics of, evaluation of, (Clinical Volume 6, Chapter 75) 
neuroblastic intracranial malignancy, (Foundations Volume 3, Chapter 62) 
optic nerve involvement, (Foundations Volume 3, Chapter 16) 
orbital exenteration in, (Clinical Volume 6, Chapter 109) 
orbital extension of, (Clinical Volume 2, Chapter 46) 
13 q-deletion syndrome and, (Clinical Volume 6, Chapter 75) 
radiation therapy for
episclereal plaque and, (Clinical Volume 6, Chapter 109) 
rosettes and photoreceptor differentiation and, (Foundations Volume 3, Chapter 21) 
second primary tumors and, (Foundations Volume 3, Chapter 62) 
subconjunctival chemoreduction of, (Clinical Volume 6, Chapter 109) 
treatment of, (Clinical Volume 3, Chapter 35) (Clinical Volume 6, Chapter 75)  (Clinical Volume 6, Chapter 109 ) 
assessment of response to, (Clinical Volume 6, Chapter 109) 
chemoreduction in
combined modalities in, (Clinical Volume 6, Chapter 109) 
enucleation in. (See Retinoblastoma, enucleation for)
episcleral plaque radiotherapy in, (Clinical Volume 6, Chapter 109) 
general considerations in, (Clinical Volume 6, Chapter 109) 
orbital exenteration in, (Clinical Volume 6, Chapter 109) 
trilateral retinoblastoma, (Foundations Volume 3, Chapter 62) 
ultrasonography of, (Clinical Volume 3, Chapter 3) 
Retinoblastoma gene
physical properties, (Foundations Volume 3, Chapter 62) 
13q14 syndrome and, (Foundations Volume 3, Chapter 62) 
Retinocerebellar angiomatosis, (Clinical Volume 2, Chapter 17) See also Von Hippel–Lindau disease, (Clinical Volume 2, Chapter 17) 
Retinochoroidal coloboma, (Clinical Volume 3, Chapter 8) 
Retinochoroidal infarction, neurosurgery and, (Clinical Volume 2, Chapter 5) 
Retinochoroidectomy, internal of Peyman, (Clinical Volume 4, Chapter 36) 
Retinochoroiditis. See also Chorioretinitis
Retinochoroiditis, toxoplasmic, (Clinical Volume 5, Chapter 32) 
Retinofugal projections, (Clinical Volume 2, Chapter 4) 
Retino-geniculo-striate pathway, (Clinical Volume 2, Chapter 7) 
Retino-geniculo-striate pathway lesions, (Clinical Volume 2, Chapter 7) 
Anton’s syndrome, (Clinical Volume 2, Chapter 7) 
artifact, blindsight, (Clinical Volume 2, Chapter 7) 
blind, normal hemifields, interactions between, (Clinical Volume 2, Chapter 7) 
blindsight
explanations of, (Clinical Volume 2, Chapter 7) 
hemidecortication, (Clinical Volume 2, Chapter 7) 
residual vision, (Clinical Volume 2, Chapter 7) 
blindsight phenomena, varieties of, (Clinical Volume 2, Chapter 7) 
cerebral blindness, (Clinical Volume 2, Chapter 7) 
homonymous defects, rehabilitation of, (Clinical Volume 2, Chapter 7) 
lateral geniculate nucleus, (Clinical Volume 2, Chapter 7) 
optic radiations, (Clinical Volume 2, Chapter 7) 
striate lesions, visual field defects from, (Clinical Volume 2, Chapter 7) 
visual field, abnormalities in, (Clinical Volume 2, Chapter 7) 
Retinoic acid
in human papillomavirus, (Foundations Volume 2, Chapter 95) 
Retinoid processing, (Foundations Volume 1, Chapter 21) 
Retinoids. See also specific drugs
teratogenicity of, (Clinical Volume 5, Chapter 39) 
Retinol. See Vitamin A
Retinol binding protein (RBP), (Clinical Volume 5, Chapter 59) 
Retinol deficiency, (Clinical Volume 2, Chapter 5) 
Retinol ester, in eye, (Clinical Volume 1, Chapter 72C) 
Retinopathy. See also Vitreoretinopathy
in Bardet-Biedl syndrome, (Clinical Volume 5, Chapter 31) 
of blood dyscrasias, (Clinical Volume 3, Chapter 18 ) 
chemotherapeutic agents and, (Clinical Volume 2, Chapter 5) 
diabetic, (Foundations Volume 3, Chapter 1) (Foundations Volume 3, Chapter 18) 
contrast sensitivity in, (Clinical Volume 1, Chapter 35) 
differential diagnosis of, (Clinical Volume 3, Chapter 30) 
electrophysiologic abnormalities in, (Clinical Volume 3, Chapter 30) 
epiretinal membranes in, (Clinical Volume 6, Chapter 56) 
fluorescein angiography, (Foundations Volume 2, Chapter 113D ) 
lenticular fluorescence and, (Clinical Volume 1, Chapter 31) 
media opacities in, (Clinical Volume 6, Chapter 56) 
platelet dysfunction and, (Clinical Volume 5, Chapter 23) 
retinal blood flow, (Foundations Volume 2, Chapter 5) 
digitalis toxicity and, (Clinical Volume 2, Chapter 5) 
distant extraocular trauma and, (Clinical Volume 3, Chapter 32 ) 
dominant familial exudative, photocoagulation in, (Clinical Volume 6, Chapter 76) 
herpes zoster. (See also Herpes zoster)
in herpes zoster ophthalmicus, (Clinical Volume 4, Chapter 20) 
HIV, cytomegalovirus retinitis versus, (Clinical Volume 3, Chapter 28A) 
occult outer zonal, (Clinical Volume 4, Chapter 49) 
in pancreatitis, acute, (Clinical Volume 5, Chapter 30) 
paraneoplastic, (Clinical Volume 5, Chapter 34) 
Snellen charts and, (Clinical Volume 1, Chapter 73B) 
in pregnancy-induced hypertension, (Clinical Volume 5, Chapter 32) 
of prematurity. (See Retinopathy of prematurity (retrolental fibroplasia))
proliferative, (Clinical Volume 3, Chapter 39) See also Vitreoretinopathy, proliferative
diabetic. (See Retinopathy, diabetic)
peripheral, fluorescein angiography, (Foundations Volume 2, Chapter 113C) 
radiation-induced, (Clinical Volume 3, Chapter 36A) See also Retinopathy, radiation
sickle, (Clinical Volume 3, Chapter 17) See also Sickle cell disease
Purtscher’s-like
cotton-wool spots in, (Clinical Volume 3, Chapter 14) 
labor and delivery and, (Clinical Volume 5, Chapter 32) 
radiation, (Clinical Volume 3, Chapter 36A)  (Clinical Volume 4, Chapter 44) 
background (nonproliferative), (Clinical Volume 3, Chapter 36A) 
clinical features of, 3–8, (Clinical Volume 3, Chapter 36A) 
diabetes mellitus and, (Clinical Volume 3, Chapter 36A) 
differential diagnosis of, (Clinical Volume 3, Chapter 36A) 
fluorescein angiography of, (Clinical Volume 3, Chapter 36A) 
indocyanine green angiography of, (Clinical Volume 3, Chapter 36A) 
orbital lymphoma and, (Clinical Volume 2, Chapter 39) 
pathophysiology of, 2, (Clinical Volume 3, Chapter 36A) 
photocoagulation in, (Clinical Volume 6, Chapter 76) 
radiation dosage and, (Clinical Volume 3, Chapter 36A) 
in renal failure, (Clinical Volume 5, Chapter 31) 
sarcoid, photocoagulation in, (Clinical Volume 6, Chapter 76) 
sickle cell, (Foundations Volume 3, Chapter 13) (Clinical Volume 3, Chapter 17) See also Sickle cell disease
photocoagulation in, (Clinical Volume 6, Chapter 76) 
surface wrinkling in. (See Epiretinal membranes)
of systemic lupus erythematosus, (Clinical Volume 3, Chapter 14) 
talc, photocoagulation in, (Clinical Volume 6, Chapter 76) 
tamoxifen causing, (Clinical Volume 2, Chapter 5) 
traumatic asphyxia and, (Clinical Volume 3, Chapter 32) 
visual evoked potential, (Foundations Volume 2, Chapter 105) 
vitreoschisis in, (Clinical Volume 6, Chapter 51) 
psychophysical abnormalities in, (Clinical Volume 3, Chapter 30) 
radiation retinopathy and, (Clinical Volume 3, Chapter 36A) 
retinal detachment of, prognosis for, (Clinical Volume 6, Chapter 56) 
retinal neovascularization in, (Clinical Volume 6, Chapter 56) 
Retinopathy of prematurity (retrolental fibroplasia), (Clinical Volume 3, Chapter 20)  (Clinical Volume 3, Chapter 39) 
advanced stages of, treatment of
laser photocoagulation in, (Clinical Volume 6, Chapter 108) 
scleral buckle in, (Clinical Volume 6, Chapter 108) 
international classification of, (Clinical Volume 6, Chapter 108) 
light toxicity and, (Clinical Volume 3, Chapter 37) 
photocoagulation in, (Clinical Volume 6, Chapter 76) 
retinal detachment in, surgical management of, (Clinical Volume 6, Chapter 56) (Clinical Volume 6, Chapter 72) 
treatment of, vitrectomy in, (Clinical Volume 6, Chapter 56) 
Retinopexy, pneumatic, anesthesia for, (Clinical Volume 6, Chapter 1) 
Retinoscopy, (Clinical Volume 1, Chapter 37 ) 
in craniofacial syndromes, (Clinical Volume 6, Chapter 110) 
with cross cylinder, (Clinical Volume 1, Chapter 38) 
in evaluating fit of soft contact lenses, (Clinical Volume 1, Chapter 55) 
“oil droplet” reflex in, (Clinical Volume 5, Chapter 31) 
Retinotomy
drainage of subretinal fluid in, (Clinical Volume 6, Chapter 56) 
for retinal traction release, (Clinical Volume 6, Chapter 56) 
subretinal access in, (Clinical Volume 6, Chapter 56) 
Retinotopic motion defects, (Foundations Volume 2, Chapter 22) 
Retraction of eyelids. See Lids, retraction of
Retraction syndrome, Duane, (Foundations Volume 3, Chapter 59) 
Retractors, eyelid, (Clinical Volume 5, Chapter 72) 
Retroblepharoplasty, (Clinical Volume 5, Chapter 74) 
Retrobulbar anesthesia, (Clinical Volume 6, Chapter 1) 
intraocular pressure effects of, (Foundations Volume 2, Chapter 7) 
Retrochiasmal lesions, and visual evoked potential, (Foundations Volume 2, Chapter 105) 
Retrochiasmal visual pathways, (Clinical Volume 2, Chapter 7) 
cerebral visual loss, (Clinical Volume 2, Chapter 7) 
occipito-parietal pathway disorders, (Clinical Volume 2, Chapter 7) 
Balint’s syndrome, (Clinical Volume 2, Chapter 7) 
cerebral akinetopsia, (Clinical Volume 2, Chapter 7) 
occipito-temporal pathway disorders, (Clinical Volume 2, Chapter 7) 
alexia, (Clinical Volume 2, Chapter 7) 
alexia with agraphia, (Clinical Volume 2, Chapter 7) 
assessment of reading, (Clinical Volume 2, Chapter 7) 
attention, reading, (Clinical Volume 2, Chapter 7) 
central dyslexia, (Clinical Volume 2, Chapter 7) 
eye movements, reading, (Clinical Volume 2, Chapter 7) 
secondary alexia, (Clinical Volume 2, Chapter 7) 
visual loss, reading, (Clinical Volume 2, Chapter 7) 
color processing, (Clinical Volume 2, Chapter 7) 
cerebral dyschromatopsia, (Clinical Volume 2, Chapter 7) 
color anomia, agnosia, (Clinical Volume 2, Chapter 7) 
hemiachromatopsia, (Clinical Volume 2, Chapter 7) 
testing achromatopsic patients, (Clinical Volume 2, Chapter 7) 
topographagnosia, (Clinical Volume 2, Chapter 7) 
visual agnosia, (Clinical Volume 2, Chapter 7) 
associated clinical findings, (Clinical Volume 2, Chapter 7) 
disorders of face perception, (Clinical Volume 2, Chapter 7) 
functional deficit in prosopagnosia, (Clinical Volume 2, Chapter 7) 
testing in prosopagnosia, (Clinical Volume 2, Chapter 7) 
positive visual phenomena, (Clinical Volume 2, Chapter 7) 
visual hallucinations, (Clinical Volume 2, Chapter 7) 
with altered mental states, (Clinical Volume 2, Chapter 7) 
with cognitive dysfunction, (Clinical Volume 2, Chapter 7) 
during eye closure, (Clinical Volume 2, Chapter 7) 
hallucinatory states, (Clinical Volume 2, Chapter 7) 
migrainous hallucinations, (Clinical Volume 2, Chapter 7) 
peduncular hallucinations, (Clinical Volume 2, Chapter 7) 
release hallucinations, (Clinical Volume 2, Chapter 7) 
visual seizures, (Clinical Volume 2, Chapter 7) 
visual perseveration, (Clinical Volume 2, Chapter 7) 
cerebral polyopia, (Clinical Volume 2, Chapter 7) 
retino-geniculo-striate pathway lesions, (Clinical Volume 2, Chapter 7) 
Anton’s syndrome, (Clinical Volume 2, Chapter 7) 
artifact, blindsight, (Clinical Volume 2, Chapter 7) 
blind, normal hemifields, interactions between, (Clinical Volume 2, Chapter 7) 
blindsight phenomena, varieties of, (Clinical Volume 2, Chapter 7) 
cerebral blindness, (Clinical Volume 2, Chapter 7) 
hemidecortication, (Clinical Volume 2, Chapter 7) 
homonymous defects, rehabilitation of, (Clinical Volume 2, Chapter 7) 
lateral geniculate nucleus, (Clinical Volume 2, Chapter 7) 
optic radiations, (Clinical Volume 2, Chapter 7) 
striate lesions, visual field defects from, (Clinical Volume 2, Chapter 7) 
visual field, abnormalities in, (Clinical Volume 2, Chapter 7) 
Retrocorneal membrane, after penetrating keratoplasty, (Clinical Volume 6, Chapter 26) 
Retroequatorial myopexy, (Clinical Volume 6, Chapter 91) See also Fadenoperation
Retrograde axonal transport, (Foundations Volume 1, Chapter 19) 
Retrograde prosopagnosia, (Foundations Volume 2, Chapter 22) 
Retroillumination, in cataract detection and monitoring, (Clinical Volume 1, Chapter 73B) (Clinical Volume 3, Chapter 33) 
Retrolamina, optic nerve, (Foundations Volume 1, Chapter 25) 
Retrolental fibroplasia. See Retinopathy of prematurity (retrolental fibroplasia)
Retrolental fibroplasia (RLF), (Foundations Volume 1, Chapter 15) 
Retrolental space, cells in, in uveitis, (Clinical Volume 4, Chapter 32) 
Reverse Duane syndrome, (Clinical Volume 2, Chapter 12) 
Reverse transcription-polymerase chain reaction, (Foundations Volume 2, Chapter 40B) 
Rev-Eyes. See Dapirazole
Rey-Osterreith Complex Figure Test, (Clinical Volume 2, Chapter 7) 
RFLP (restrictive fragment length polymorphism), (Foundations Volume 3, Chapter 55) 
Rhabdomyoma, in tuberous sclerosis, (Clinical Volume 5, Chapter 36) 
Rhegmatogenous retinal detachment. See Retinal detachment, rhegmatogenous
Rheumatic diseases. See also specific disease
ocular manifestations of, (Clinical Volume 5, Chapter 26 ) 
Rheumatic valvular disease, retinal arterial occlusions and, (Clinical Volume 2, Chapter 5) 
Rheumatoid arthritis, (Clinical Volume 5, Chapter 26)  See Arthritis, rheumatoid
clinical features of, (Clinical Volume 5, Chapter 26) 
ocular manifestations of, (Clinical Volume 5, Chapter 26) 
superior oblique tendon sheath syndrome and, (Clinical Volume 1, Chapter 20) 
Rheumatoid diseases, immunology, (Foundations Volume 2, Chapter 33 ) 
Rh incompatibility, (Foundations Volume 2, Chapter 25) 
Rhinitis, allergic, (Foundations Volume 2, Chapter 34) 
upper respiratory tract infection versus, in children, (Clinical Volume 6, Chapter 81) 
Rhinoconjunctivitis, allergic, (Clinical Volume 4, Chapter 2 ) 
Rhino-orbital mucormycosis, (Clinical Volume 2, Chapter 28) 
Rhinoplasty, dacryostenosis after, (Clinical Volume 4, Chapter 13) 
Rhinosporidium seeberi, (Foundations Volume 3, Chapter 4) 
Rhodamine-auramine, (Foundations Volume 2, Chapter 40) 
Rhodamine-auramine stain, (Foundations Volume 2, Chapter 40) 
Rhomboid flap, in lid repair, (Clinical Volume 5, Chapter 88) 
Riboflavin
cataract risk reduction and, (Clinical Volume 1, Chapter 72C) 
Ribonucleic acid (RNA) probes, in optic nerve, (Foundations Volume 2, Chapter 40) (Foundations Volume 3, Chapter 51) 
Richner-Hanhart syndrome, (Clinical Volume 4, Chapter 15) See also Tyrosinemia
Richter transformation, (Clinical Volume 2, Chapter 39) 
Rifabutin, ophthalmic side effects of, (Clinical Volume 4, Chapter 58) 
Rifles, air, eye injuries from, protective device effectiveness and, (Clinical Volume 5, Chapter 45) 
Rift Valley fever retinitis (RVFR), (Clinical Volume 4, Chapter 45) 
Rift Valley fever virus, (Foundations Volume 2, Chapter 85) 
Riluzole, neuroprotection of axons and, (Clinical Volume 3, Chapter 57) 
Ring abscess, Pseudomonas aeruginosa and, (Clinical Volume 4, Chapter 18) 
Rink hockey, eye injuries from, protective device effectiveness and, (Clinical Volume 5, Chapter 45) 
Rizatriptan, for migraine, (Clinical Volume 2, Chapter 16) 
RLF. See Retrolental fibroplasia
RNA. See Ribonucleic acid
Robin syndrome. See Pierre Robin syndrome
Rochaelimaea quintana, (Foundations Volume 2, Chapter 58) 
Rocky Mountain spotted fever, 2, (Foundations Volume 2, Chapter 58) 
Rod-cone dystrophy. See Cone-rod dystrophies
Rod disc membranes, retina and, (Foundations Volume 2, Chapter 12) 
Rod monochromaticism, (Clinical Volume 2, Chapter 5) 
complete form of, (Clinical Volume 3, Chapter 9) 
incomplete form of, (Clinical Volume 3, Chapter 9) 
Rod outer segment membranes, retina and, (Foundations Volume 2, Chapter 12) 
Rod outer segment obstruction, glaucoma and, (Clinical Volume 3, Chapter 54E) 
Rod plasma membranes, retina and, (Foundations Volume 2, Chapter 12) 
Rods, (Clinical Volume 2, Chapter 4) (Foundations Volume 2, Chapter 12) See also Photoreceptor(s)
characteristics of, (Foundations Volume 1, Chapter 19) 
circuit, in starlight, (Foundations Volume 2, Chapter 13) 
cones. (See Photoreceptors, retinaland)
cones and
interaction between signals, (Foundations Volume 2, Chapter 13) 
disc membranes, chemistry, (Foundations Volume 2, Chapter 12) 
outer segments
membrane biosynthesis and turnover, (Foundations Volume 2, Chapter 12) 
plasma membranes, chemistry, (Foundations Volume 2, Chapter 12) 
Roentgenogram, plain, in orbital disease evaluation, (Clinical Volume 2, Chapter 23) See also Orbit, diseases of, plain roentgenogram in evaluation of
Roentgenology. See Radiology
Romberg syndrome. See Parry-Romberg syndrome
Romberg test, (Clinical Volume 2, Chapter 18) 
“sharpened, ”, (2) 18: 10
ROP. See Retinopathy of prematurity (retrolental fibroplasia)
Rosacea. See Acne rosacea
Rosai-Dorfman disease, (Clinical Volume 2, Chapter 39) 
Rose bengal stain, in herpes simplex keratitis, (Clinical Volume 4, Chapter 19) 
Rosenthal fibers, in optic nerve gliomas, (Clinical Volume 2, Chapter 42) 
Rosettes, of retinoblastoma, (Foundations Volume 3, Chapter 21) 
Rostral interstitial nucleus of medial longitudinal fasciculus
Rotary chair test, (Clinical Volume 2, Chapter 18) 
Rotary nystagmus, (Clinical Volume 2, Chapter 11) 
Rotational nystagmus, (Clinical Volume 2, Chapter 11) 
Rotational tests, for eye movements in infants, (Clinical Volume 2, Chapter 3) 
Rotation flaps, in lid repair, (Clinical Volume 5, Chapter 88) 
Rotations
ocular motility and, (Foundations Volume 2, Chapter 23) 
Roth-Bielschowsky deviation. See Oculocephalic reflex
Rothmund-Thomson syndrome, (Clinical Volume 5, Chapter 41) 
Roth spots, retinal, (Clinical Volume 3, Chapter 7) 
Rough endoplasmic reticulum (RER), in ciliary body, (Foundations Volume 1, Chapter 13) 
Routine visual fields, (Clinical Volume 3, Chapter 33) 
Roveda procedure, in telecanthus correction, (Clinical Volume 6, Chapter 110) 
RPE. See Retinal pigment epithelium
RP3 gene, recessive, X-linked, (Clinical Volume 3, Chapter 2) 
Rubella syndrome, (Clinical Volume 3, Chapter 55) 
Rubenstein-Taybi syndrome, (Foundations Volume 3, Chapter 59) 
Duane retraction syndrome and, (Clinical Volume 1, Chapter 20) 
Rubeosis iridis, (1)18: 3; 19: 10; (Clinical Volume 3, Chapter 54E) (Clinical Volume 5, Chapter 20) 
proliferative diabetic retinopathy and, (Clinical Volume 6, Chapter 76) 
in retinal vein occlusion, (Clinical Volume 3, Chapter 15) 
Rubinstein-Taybi syndrome, (Clinical Volume 5, Chapter 41) 
Rufous oculocutaneous albinism, (Clinical Volume 4, Chapter 38) 
Rugby, eye injuries from, protective device effectiveness and, (Clinical Volume 5, Chapter 45) 
Running, eye injuries from, protective device effectiveness and, (Clinical Volume 5, Chapter 45) 
Rupture, trauma and, (Clinical Volume 4, Chapter 61 ) 
Rushton ocular measurements, (Clinical Volume 1, Chapter 33) 
Rust spots, in eye, (Clinical Volume 4, Chapter 62) 
RVFR (Rift Valley fever retinitis), (Clinical Volume 4, Chapter 45) 

 Back to Top

Subject Index S
Sabin-Feldman dye test, in toxoplasmosis, (Clinical Volume 4, Chapter 46) 
Sabouraud agar, (Clinical Volume 6, Chapter 64) 
for cultures in fungal keratitis, (Clinical Volume 4, Chapter 18) 
Sabouraud dextrose agar, (Foundations Volume 2, Chapter 40) 
Saccade generation, (Clinical Volume 2, Chapter 10) 
Saccades, (Foundations Volume 1, Chapter 38) 
abnormalities of, (Clinical Volume 1, Chapter 4) 
cortical control of, (Clinical Volume 2, Chapter 10) 
generation of, cortical areas contributing to, (Foundations Volume 1, Chapter 38) 
in Huntington disease, (Clinical Volume 2, Chapter 10) 
internal monitor of, (Clinical Volume 2, Chapter 9) 
palsy, congenital, (Clinical Volume 2, Chapter 10) 
pulse/pulse trains, (Clinical Volume 2, Chapter 11) 
pursuit system and, (Clinical Volume 2, Chapter 10) 
reading impairment due to, (Clinical Volume 2, Chapter 7) 
superior colliculus and, (Clinical Volume 2, Chapter 10) 
velocity measurement in, (Clinical Volume 1, Chapter 21 ) 
in abducens nerve palsy, (Clinical Volume 1, Chapter 21) 
in Alzheimer’s disease, (Clinical Volume 1, Chapter 21) 
in Brown syndrome, (Clinical Volume 1, Chapter 21) 
in chronic progressive external ophthalmoplegia, (Clinical Volume 1, Chapter 21) 
in disinserted extraocular muscle, (Clinical Volume 1, Chapter 21) 
in divergence paralysis, (Clinical Volume 1, Chapter 21) 
in double elevator palsy, (Clinical Volume 1, Chapter 21) 
in Duane syndrome, (Clinical Volume 1, Chapter 21) 
electrode placement in, (Clinical Volume 1, Chapter 21) 
electro-oculography technique and normal values for, (Clinical Volume 1, Chapter 21) 
in extraocular muscle palsy, (Clinical Volume 1, Chapter 21) 
infra-red oculography in, (Clinical Volume 1, Chapter 21) 
in internuclear ophthalmoplegia, (Clinical Volume 1, Chapter 21) 
in limited downward gaze, (Clinical Volume 1, Chapter 21) 
in miscellaneous disorders, (Clinical Volume 1, Chapter 21) 
in Mobius syndrome, (Clinical Volume 1, Chapter 21) 
muscle transposition surgery and, (Clinical Volume 1, Chapter 21) 
in neuro-ophthalmic disorders, (Clinical Volume 1, Chapter 21) 
in oculomotor nerve palsy, (Clinical Volume 1, Chapter 21) 
in orbital floor fracture, (Clinical Volume 1, Chapter 21) 
paralysis versus restriction and, (Clinical Volume 1, Chapter 21) 
in sixth nerve palsy, (Clinical Volume 6, Chapter 84) 
in superior oblique palsy, (Clinical Volume 1, Chapter 21) 
in thyroid ophthalmopathy, (Clinical Volume 1, Chapter 21) 
Saccades, roles for, (Clinical Volume 2, Chapter 10) 
Saccadic localization, in blindsight, (Foundations Volume 2, Chapter 22) 
Saccadic targeting, inaccuracies in, (Clinical Volume 2, Chapter 7) 
Saccular aneurysms, (Clinical Volume 2, Chapter 17) 
anterior communicating artery, (Clinical Volume 2, Chapter 17) 
carotid-ophthalmic artery, (Clinical Volume 2, Chapter 17) 
carotid-supraclinoid, (Clinical Volume 2, Chapter 17) 
intracavernous carotid, (Clinical Volume 2, Chapter 17) 
middle cerebral artery, (Clinical Volume 2, Chapter 17) 
ophthalmic artery, (Clinical Volume 2, Chapter 17) 
posterior cerebral artery, (Clinical Volume 2, Chapter 17) 
posterior communicating artery, (Clinical Volume 2, Chapter 17) 
vertebrobasilar system, (Clinical Volume 2, Chapter 17) 
Sacroiliac joint, radiology of, in uveitis, (Clinical Volume 4, Chapter 37) 
Saethre-Chotzen syndrome, (Clinical Volume 6, Chapter 110) See also Craniofacial anomalies; (Foundations Volume 1, Chapter 41) 
Sahlgren Saturation Test, (Clinical Volume 2, Chapter 7) 
Sakati-Nyhan-Tisdale syndrome, (Foundations Volume 1, Chapter 41) 
Salford Electric Instruments photometer, (Foundations Volume 2, Chapter 15) 
Salicylates
as anti-inflammatory agents. (See Nonsteroidal anti-inflammatory drugs (NSAIDs))
toxicity, carbonic anhydrase inhibitors and, (Foundations Volume 3, Chapter 30) 
Saline
hypertonic
for corneal edema, (Clinical Volume 4, Chapter 16A) 
Salivary glands
function, facial nerve and, (Foundations Volume 1, Chapter 37) 
Salmon patches
in sickle cell disease, (Clinical Volume 3, Chapter 17) 
“Salt and pepper” appearance, of RPE, in cytomegalovirus retinitis, (Clinical Volume 3, Chapter 28A) 
Salt-and-pepper fundus, (Clinical Volume 3, Chapter 7) 
Sansert (methysergide)
for cluster headache, (Clinical Volume 2, Chapter 16) 
Santavuori-Haltia disease, (Foundations Volume 3, Chapter 54B) 
S-antigen, in uveitis, (Clinical Volume 4, Chapter 54) 
Sarcoidosis, (Clinical Volume 4, Chapter 57) (Foundations Volume 2, Chapter 34) (Foundations Volume 3, Chapter 1) (Foundations Volume 3, Chapter 4) (Foundations Volume 3, Chapter 9) (Foundations Volume 3, Chapter 17) 
anterior uveitis in, (Clinical Volume 3, Chapter 54D) 
chiasmal infiltration by, (Clinical Volume 2, Chapter 6) 
conjunctivitis in, (Foundations Volume 3, Chapter 8) 
cranial nerve palsy in, (Clinical Volume 2, Chapter 12) 
differential diagnosis, (Clinical Volume 2, Chapter 35) 
facial nerve and, (Clinical Volume 2, Chapter 8) 
fluorescein angiography in, (Clinical Volume 4, Chapter 57) 
immune response in, (Clinical Volume 2, Chapter 35) 
intermediate uveitis in, (Clinical Volume 4, Chapter 43) 
lacrimal gland in, (Clinical Volume 2, Chapter 35) 
optic nerve involvement, (Foundations Volume 3, Chapter 16) 
orbital manifestations of, (Foundations Volume 3, Chapter 17) 
Sarcoid retinal vasculitis, (Foundations Volume 2, Chapter 113E) 
Sattler layer, of choroid, (Clinical Volume 4, Chapter 31) 
Saturation in color vision, testing of, (Clinical Volume 2, Chapter 7) (Clinical Volume 3, Chapter 6) 
Saturn ring, in osteogenesis imperfecta, (Clinical Volume 5, Chapter 29) 
Scalded skin syndrome, (Clinical Volume 5, Chapter 27) See also Toxic epidermal necrolysis
Scanning laser ophthalmoscopes, indocyanine green angiography based on, (Clinical Volume 3, Chapter 4A) 
Scanning laser ophthalmoscopy
confocal
optic nerve topography and, (Foundations Volume 2, Chapter 111 ) 
normal versus abnormal, (Foundations Volume 2, Chapter 111) 
reproducibility of measurements, (Foundations Volume 2, Chapter 111) 
visual function measures versus, (Foundations Volume 2, Chapter 111) 
ICG angiography and, (Foundations Volume 2, Chapter 110) 
Scanning laser polarimetry, in glaucoma, (Clinical Volume 3, Chapter 52) 
Scar formation
after lid trauma repair
early management of, (Clinical Volume 5, Chapter 75) 
keratotomy incision and, intersecting, (Clinical Volume 6, Chapter 42) 
macular, disciform, (Clinical Volume 3, Chapter 7) 
in pemphigoid, cicatricial, 5, (Clinical Volume 5, Chapter 27) 
pigment epithelium in, (Clinical Volume 3, Chapter 7) 
in toxoplasmic retinochoroiditis, (Clinical Volume 4, Chapter 46) 
Scarring, corneal, postinflammatory, ultrasound biomicroscopy, (Foundations Volume 2, Chapter 106) 
Scattering, light. See Light scattering
SC disease, (Clinical Volume 3, Chapter 17) See also Sickle cell disease
Schafer syndrome, cataract in, (Clinical Volume 5, Chapter 41) 
Scheie angle classification system, (Clinical Volume 3, Chapter 44) 
Scheie stripe (Scheie line), (Clinical Volume 3, Chapter 54B) 
Scheimpflug cameras, in cataract detection and monitoring, (Clinical Volume 1, Chapter 31) 
Scheimpflug principle, (Clinical Volume 1, Chapter 31) 
Scheiner theories, (Clinical Volume 1, Chapter 33) 
Schematic eye, (Clinical Volume 1, Chapter 33 ) 
historical aspects of, (Clinical Volume 1, Chapter 33) 
positions of ocular surfaces and, (Clinical Volume 1, Chapter 33) 
radii of curvature of surfaces and, (Clinical Volume 1, Chapter 33) 
refractive indices and, (Clinical Volume 1, Chapter 33) 
Scheuthauer-Marie Sainton syndrome, (Foundations Volume 3, Chapter 17) 
Schindler disease
ocular findings in, (Clinical Volume 5, Chapter 19) 
type 1, ophthalmologic features of, (Clinical Volume 5, Chapter 19) 
Schiotz tonometer, 2, (Clinical Volume 3, Chapter 46) 
Schirmer test, (Foundations Volume 2, Chapter 3) (Clinical Volume 4, Chapter 13) 
in allergic conjunctivitis, (Clinical Volume 4, Chapter 2) 
in keratoconjunctivitis sicca, (Clinical Volume 2, Chapter 35) 
for lacrimation defects, (Clinical Volume 4, Chapter 13) 
in myotonic dystrophy, (Clinical Volume 5, Chapter 29) 
Schirmer test of tear function, (Clinical Volume 2, Chapter 8) 
Schisis
retinal. (See Retinoschisis)
vitreous. (See Vitreoschisis)
Schnaitmann bifocals, (Clinical Volume 1, Chapter 44) 
Schocket tube, 2, 4, (Clinical Volume 6, Chapter 17) 
Schott lid speculum, (Clinical Volume 6, Chapter 3) 
Schultze, fiber basket of, retinal, (Clinical Volume 3, Chapter 1) 
Schwalbe
contraction folds of, (Foundations Volume 1, Chapter 11) 
structural folds of, (Foundations Volume 1, Chapter 11) 
Schwalbe contraction plicae, (Foundations Volume 1, Chapter 1) 
Schwalbe line cells, (Foundations Volume 1, Chapter 10) 
Schwartz-Matsuo syndrome, (Foundations Volume 3, Chapter 19) 
Schwartz syndrome, (Clinical Volume 3, Chapter 54E) 
SCID (severe combined immunodeficiency disease), (Clinical Volume 5, Chapter 40) 
Scintigraphy, technetium-99m-labeled RBC, of capillary hemangioma, (Clinical Volume 2, Chapter 27) 
Sclera, (Foundations Volume 1, Chapter 23)  (Foundations Volume 2, Chapter 4)  (Foundations Volume 3, Chapter 9) See also Episclera, (Foundations Volume 1, Chapter 23) (Foundations Volume 2, Chapter 4) 
anterior, disorders, ultrasound biomicroscopy, (Foundations Volume 2, Chapter 106) 
blood supply, emissary canals, (Foundations Volume 1, Chapter 23) 
congenital anomalies, (Foundations Volume 3, Chapter 9) 
conjunctiva and, barrier function, (Foundations Volume 2, Chapter 61) 
intraocular pressure and, (Foundations Volume 2, Chapter 4) 
lymphatic drainage, (Foundations Volume 1, Chapter 23) 
necrosis, after retinal reattachment, (Foundations Volume 3, Chapter 6) 
plaques
hyaline, ultrasound biomicroscopy, (Foundations Volume 2, Chapter 106) 
postnatal development, (Foundations Volume 1, Chapter 23) 
prenatal development, (Foundations Volume 1, Chapter 23) 
scleral foramina, (Foundations Volume 1, Chapter 23) 
anterior scleral foramen, (Foundations Volume 1, Chapter 23) 
posterior scleral foramen, (Foundations Volume 1, Chapter 23) 
surface anatomy of, (Foundations Volume 1, Chapter 1) 
transplantation, antimicrobial prophylaxis, (Foundations Volume 2, Chapter 64) 
vascular system of, (Foundations Volume 1, Chapter 1) 
Sclera and episclera, (Clinical Volume 4, Chapter 23)  (Clinical Volume 4, Chapter 61) (Clinical Volume 5, Chapter 34) (Clinical Volume 6, Chapter 15) 
bare, in pterygium excision, (Clinical Volume 6, Chapter 35) 
blue, (Clinical Volume 4, Chapter 23) 
in Hallermann-STreiff syndrome, (Clinical Volume 5, Chapter 29) 
in Marfan’s syndrome, (Clinical Volume 5, Chapter 29) 
in osteogenesis imperfecta, (Clinical Volume 5, Chapter 29) 
buckling. (See Scleral buckling surgery)
chemical injury of, (Clinical Volume 4, Chapter 23) 
congenital anomalies of, (Clinical Volume 4, Chapter 23) 
degenerations of, (Clinical Volume 4, Chapter 23) 
dissection of, in scleral buckling, (Clinical Volume 6, Chapter 59) 
encroachment of, on cornea, (Clinical Volume 4, Chapter 23) 
episcleral plaque radiotherapy of, in retinoblastoma, (Clinical Volume 6, Chapter 109 ) 
in Fadenoperation, (Clinical Volume 6, Chapter 91) 
flaps, disinsertion, glaucoma filtering surgery and, (Clinical Volume 6, Chapter 24) 
fluorescein angiography of, anterior segment, (Clinical Volume 4, Chapter 23) 
arterial phase of, (Clinical Volume 4, Chapter 23) 
capillary phase of, (Clinical Volume 4, Chapter 23) 
episcleral arterial circle in, 4, (Clinical Volume 4, Chapter 23) 
episcleral circulation and, 4, (Clinical Volume 4, Chapter 23) 
limbal arcades in, (Clinical Volume 4, Chapter 23) 
gastrointestinal disorders involving, (Clinical Volume 5, Chapter 30) 
graft of
double-plate shunt placement and, (Clinical Volume 6, Chapter 17) 
hemangioma of, (Clinical Volume 4, Chapter 23) 
in Sturge-Weber syndrome, (Clinical Volume 5, Chapter 36) 
history taking and, (Clinical Volume 4, Chapter 23) 
hyaline plaques of, senile, (Clinical Volume 4, Chapter 23) 
in hypercalcemia, (Clinical Volume 4, Chapter 23) 
incisions of, in cataract surgery, pediatric, (Clinical Volume 6, Chapter 100) 
inflammation of, (Clinical Volume 4, Chapter 23) See also Episcleritis; Scleritis
lacerations of, repair of, (Clinical Volume 6, Chapter 39) 
patch graft of, double-plate shunt placement and, (Clinical Volume 6, Chapter 17) 
in pathologic myopia, (Clinical Volume 3, Chapter 36) 
perforation of, (Clinical Volume 6, Chapter 83) 
fibrous ingrowth in, (Clinical Volume 3, Chapter 7) 
intercalary, spontaneous, (Clinical Volume 4, Chapter 23) 
in scleral buckling surgery, (Clinical Volume 6, Chapter 59) 
rhabdomyosarcoma of, (Clinical Volume 4, Chapter 23) 
rupture of, traumatic, (Clinical Volume 3, Chapter 31) 
scleritis of, (Clinical Volume 4, Chapter 23) See also Scleritis
venous pressure, glaucoma and, (Clinical Volume 3, Chapter 54E) 
in Vogt-Koyanagi-Harada syndrome, (Clinical Volume 4, Chapter 23) 
in xanthomatosis, (Clinical Volume 4, Chapter 23) 
Scleral bed, exposure
Baerveldt tube implantation in, (Clinical Volume 6, Chapter 17) 
double-plate shunt placement in, (Clinical Volume 6, Chapter 17) 
Scleral buckling, (Clinical Volume 6, Chapter 59) 
anatomic results after, (Clinical Volume 6, Chapter 59) 
chorioretinal folds caused by, (Clinical Volume 3, Chapter 36) 
laser photocoagulation in, (Clinical Volume 6, Chapter 108) 
postoperative, glaucoma and, (Clinical Volume 3, Chapter 54E) 
pseudophakic retinal detachment, (Clinical Volume 6, Chapter 59) 
subretinal fluid, management of, (Clinical Volume 6, Chapter 59) 
surgical technique, (Clinical Volume 6, Chapter 59) 
visual results after, (Clinical Volume 6, Chapter 59) 
Scleral buckling surgery, (Foundations Volume 3, Chapter 13) (Clinical Volume 6, Chapter 59) 
in acute retinal necrosis syndrome, (Clinical Volume 3, Chapter 28) 
anterior segment ischemia after, (Clinical Volume 6, Chapter 59) 
buckle implantation in, (Clinical Volume 6, Chapter 59) 
buckling materials for, (Clinical Volume 6, Chapter 59) 
postoperative extrusion for, (Clinical Volume 6, Chapter 59) 
choroidal detachments after, (Clinical Volume 6, Chapter 59) 
color Doppler imaging after, (Foundations Volume 2, Chapter 102) 
corneal clouding during, (Clinical Volume 6, Chapter 59) 
cystoid macular edema after, (Clinical Volume 6, Chapter 59) 
encircling buckles in, (Clinical Volume 6, Chapter 59) 
explant technique in, (Clinical Volume 6, Chapter 59) 
buckling materials for, (Clinical Volume 6, Chapter 59) 
segmental versus encircling buckles in, (Clinical Volume 6, Chapter 59) 
implant techniques in, (Clinical Volume 6, Chapter 59) 
macular pucker after, (Clinical Volume 6, Chapter 59) 
in pseudophakic retinal detachment, (Clinical Volume 6, Chapter 59) 
refractive error after, changes in, (Clinical Volume 6, Chapter 59) 
retinal breaks in
scleral dissection in, (Clinical Volume 6, Chapter 59) 
segmental buckles in, (Clinical Volume 6, Chapter 59) 
subretinal fluid management in, (Clinical Volume 6, Chapter 59) 
complications during, (Clinical Volume 6, Chapter 59) 
surgical anatomy and, (Clinical Volume 6, Chapter 59) 
suture technique in, (Clinical Volume 6, Chapter 59) 
Scleral search coil, (Clinical Volume 2, Chapter 9) 
Scleral tunnel incisions, (Clinical Volume 6, Chapter 6) 
Scleritis, (Foundations Volume 3, Chapter 9) (Clinical Volume 4, Chapter 2) (Clinical Volume 4, Chapter 23)  (Clinical Volume 4, Chapter 40) See also Episcleritis
classification of, (Clinical Volume 4, Chapter 23) 
clinical features of, (Clinical Volume 4, Chapter 23 ) 
complications of, (Clinical Volume 4, Chapter 23) 
corneal changes in, (Clinical Volume 4, Chapter 23) 
corneal infiltration in, (Clinical Volume 4, Chapter 39) 
herpes simplex virus and, (Clinical Volume 4, Chapter 23) 
herpes zoster in, (Clinical Volume 4, Chapter 23) 
history of patient with, (Clinical Volume 4, Chapter 23) 
iridocyclitis and, (Clinical Volume 4, Chapter 42) 
keratitis in
keratouveitis and, (Clinical Volume 4, Chapter 39) 
limbal guttering in, (Clinical Volume 4, Chapter 23) 
optic nerve swelling in, (Clinical Volume 4, Chapter 23) 
in polyarteritis nodosa, (Clinical Volume 4, Chapter 15) 
retinal detachment in, (Clinical Volume 4, Chapter 23) 
in rheumatoid arthritis, (Clinical Volume 4, Chapter 15) 
systemic disorders with, (Clinical Volume 4, Chapter 23) 
in systemic lupus erythematosus, (Clinical Volume 4, Chapter 15) 
transparency and thinning of sclera in, (Clinical Volume 4, Chapter 23) 
treatment of, (Clinical Volume 4, Chapter 23) (Clinical Volume 4, Chapter 39) 
corticosteroids in, (Clinical Volume 4, Chapter 23) 
immunosuppressive agents in, (Clinical Volume 4, Chapter 23) 
nonsteroidal anti-inflammatory drugs in, (Clinical Volume 4, Chapter 23) 
ultrasonography in, (Clinical Volume 3, Chapter 3) 
visual acuity in, (Clinical Volume 4, Chapter 23) 
Sclerocornea plana, (Foundations Volume 1, Chapter 9) 
Sclerokeratecotmy, lamellar. See Lamellar sclerokeratectomy
Scleromalacia perforans, (Clinical Volume 4, Chapter 23) 
Sclerosing panencephalitis, subacute, (Foundations Volume 2, Chapter 32) 
Sclerosis
choroidal
in Paget’s disease, (Clinical Volume 5, Chapter 29) 
of lens and ciliary body, presbyopia from, (Clinical Volume 1, Chapter 33) 
multiple. (See Multiple sclerosis; Multiple sclerosis (MS))
progressive systemic, (Foundations Volume 2, Chapter 33) 
progressive systemic. (See Scleroderma)
tuberous. (See Tuberous sclerosis)
Sclerotic disc, senile, (Clinical Volume 3, Chapter 52) 
Sclerotomy
in nanophthalmos, (Clinical Volume 3, Chapter 53) 
in pseudophakic/aphakic eye, (Clinical Volume 6, Chapter 56) 
Sclerouvectomy, lamellar, partial, of Shields, (Clinical Volume 4, Chapter 36) 
Sclopeteria, retinitis, (Clinical Volume 3, Chapter 31) 
Scopolamine
in herpes simplex keratitis, (Clinical Volume 4, Chapter 19) 
ocular toxicity of, (Clinical Volume 5, Chapter 37) 
systemic toxicity of, (Clinical Volume 5, Chapter 37) 
Scopolamine (Hyoscine)
ocular motility and, (Foundations Volume 2, Chapter 23) 
side effects, in infants and children, (Foundations Volume 3, Chapter 43) 
Scotch tape preparation, for fungal identification, (Foundations Volume 2, Chapter 54) 
Scotomas, (Clinical Volume 2, Chapter 1) See also Field defects; See also Automated perimetry
blurring versus, (Clinical Volume 2, Chapter 2) 
central, (Clinical Volume 2, Chapter 6) 
in ischemic optic neuropathy, (Clinical Volume 2, Chapter 5) 
in nutritional optic neuropathy, (Clinical Volume 2, Chapter 5) 
in optic neuritis, (Clinical Volume 2, Chapter 5) 
in chiasmal syndromes, (Clinical Volume 2, Chapter 6) 
“junctional, ”, (2) 6: 3
in monofixation syndrome, (Clinical Volume 1, Chapter 9) 
in optic nerve disease, acquired, (Clinical Volume 2, Chapter 5) 
in pituitary disorders, (Clinical Volume 5, Chapter 21) 
scintillating, in migraine, (Foundations Volume 2, Chapter 22) 
suppression, in esotropia and exotropia, (Clinical Volume 1, Chapter 9) 
Scotopic vision. See Adaptation; Rods
Scotopic vision, rods in, (Clinical Volume 1, Chapter 33) 
Screening, (Clinical Volume 5, Chapter 54 ) 
automated perimetry in, (Clinical Volume 3, Chapter 49) 
criteria for, (Clinical Volume 5, Chapter 54 ) 
better outcome with early treatment as, (Clinical Volume 5, Chapter 54) 
cost-benefit aspects of, (Clinical Volume 5, Chapter 54) 
effectiveness and availability of treatment as, (Clinical Volume 5, Chapter 54) 
morbidity and mortality as, (Clinical Volume 5, Chapter 54) 
natural history of disease as, (Clinical Volume 5, Chapter 54) 
prevalence of disease as, (Clinical Volume 5, Chapter 54) 
screening tests in, (Clinical Volume 5, Chapter 54) 
for myasthenia gravis, (Clinical Volume 2, Chapter 12) 
ophthalmic epidemiology and, (Foundations Volume 2, Chapter 43) 
test criteria for, (Clinical Volume 5, Chapter 54) 
for von Hippel-Lindau disease, (Clinical Volume 5, Chapter 36) 
Screw clamp speculum, (Clinical Volume 6, Chapter 3) 
Scuba diving, eye injuries from, (Clinical Volume 5, Chapter 45) 
Sea blue histiocyte, syndrome of, (Foundations Volume 3, Chapter 13) 
Sea fan sign, in sickle cell retinopathy, (Clinical Volume 5, Chapter 42) 
Seasonal allergic conjunctivitis, nonsteroidal anti-inflammatory agents, (Foundations Volume 3, Chapter 38) 
Seasonal allergic conjunctivitis, NSAIDs for, (Clinical Volume 4, Chapter 2) (Foundations Volume 3, Chapter 38) 
Sebaceous carcinoma, (Foundations Volume 3, Chapter 7) 
Sebaceous cell carcinoma
orbital extension of, (Clinical Volume 2, Chapter 24) 
Sebaceous glands, lid, (Foundations Volume 1, Chapter 5) 
Seborrheic blepharitis, 2, (Clinical Volume 4, Chapter 22) 
Sec, ocular trauma and, (Clinical Volume 5, Chapter 56) 
Secobarbital, ocular toxicity of, (Clinical Volume 5, Chapter 37) 
Secondary focal plane, (Clinical Volume 1, Chapter 30) 
Secondary focal point, (Clinical Volume 1, Chapter 30) 
Secondary glaucoma, (Clinical Volume 3, Chapter 55) 
Secondary intraocular lens implantation, (Clinical Volume 6, Chapter 8) 
anterior chamber intraocular lenses, (Clinical Volume 6, Chapter 8) 
anterior chamber intraocular lens implantation, (Clinical Volume 6, Chapter 8) 
endocapsular posterior chamber lens, (Clinical Volume 6, Chapter 8) 
iris-sutured sulcus posterior chamber intraocular lens, (Clinical Volume 6, Chapter 8) 
posterior chamber intraocular lenses, (Clinical Volume 6, Chapter 8) 
preoperative screening, (Clinical Volume 6, Chapter 8) 
sulcus posterior chamber lens, (Clinical Volume 6, Chapter 8) 
surgical technique, (Clinical Volume 6, Chapter 8) 
transsclerally sulcussutured posterior chamber intraocular lens, (Clinical Volume 6, Chapter 8) 
Secondary myopathies, (Clinical Volume 5, Chapter 28) 
Second trimester ultrasound, (Foundations Volume 3, Chapter 56) 
Sectility, tissue, (Clinical Volume 6, Chapter 3) 
Sectoranopia
lateral geniculate nucleus, (Clinical Volume 2, Chapter 7) 
optic radiation, (Clinical Volume 2, Chapter 7) 
Sedative/hypnotics, ocular toxicity of, 3–4, (Clinical Volume 5, Chapter 37) 
Sedative-hypnotics, pupillary effects, (Foundations Volume 2, Chapter 9) 
Sedimentation rate. See Erythrocyte sedimentation rate
See-saw nystagmus, (Clinical Volume 2, Chapter 11) 
Seizures
in arteriovenous malformations, (Clinical Volume 2, Chapter 17) 
medications for, perioperative management of, in children, 6, (Clinical Volume 6, Chapter 81) 
in Sturge-Weber syndrome, (Clinical Volume 5, Chapter 36) 
in tuberous sclerosis, (Clinical Volume 5, Chapter 36) 
Selectins, inflammation and, (Foundations Volume 2, Chapter 27) 
Selective deficiency
of immunoglobulin isotypes, (Clinical Volume 5, Chapter 40) 
Selective laser trabeculoplasty, (Clinical Volume 1, Chapter 69B) 
Self-determination, patient right to, (Clinical Volume 5, Chapter 68) 
Self-retaining speculum, (Clinical Volume 6, Chapter 3) 
Sella turcica
empty sella syndrome and, (Clinical Volume 2, Chapter 6) 
in optic nerve gliomas, (Clinical Volume 2, Chapter 42) 
parasellar syndromes and, (Clinical Volume 2, Chapter 12) 
Semifluorinated alkane liquids
biocompatibility of, (Clinical Volume 6, Chapter 54) 
complications of, (Clinical Volume 6, Chapter 54) 
physical properties of, (Clinical Volume 6, Chapter 54) 
as vitreous substitute, (Clinical Volume 6, Chapter 54) 
Semiscleral lenses, (Clinical Volume 1, Chapter 55) 
Senile cataract. See Cataract, age-related; Cataract(s), senile
Senile sclerotic disc, in glaucoma, (Clinical Volume 3, Chapter 52) 
Senile vitritis, idiopathic, (Clinical Volume 4, Chapter 43) 
Senior-Loken syndrome, (Clinical Volume 5, Chapter 31) 
Sensitive period, of development, (Clinical Volume 1, Chapter 10) 
Sensitivity
contrast. (See Contrast sensitivity)
threshold versus, in automated perimetry, (Clinical Volume 3, Chapter 49) 
Sensitivity analysis, in cost-effectiveness studies, (Clinical Volume 5, Chapter 69) 
Sensory correspondence, (Clinical Volume 2, Chapter 13) 
Sensory esotropia, surgery for, (Clinical Volume 6, Chapter 84) 
Sensory fusion, binocular vision and. See also Fusion, binocular
Sensory receptors
Sensory system, visual
diagnosis of disorders in, in prechiasmal pathways, (Clinical Volume 2, Chapter 5) See also specific disorders
neuro-ophthalmologic examination in, (Clinical Volume 2, Chapter 2) See also under Examination
Sensory visual pathways, anatomy, physiology of, (Clinical Volume 2, Chapter 10) 
Separable acuity, minimum, (Clinical Volume 1, Chapter 33) 
Sequestered endophthalmitis, (Foundations Volume 3, Chapter 14) 
Serologic detection of antibodies, (Foundations Volume 2, Chapter 40A) 
circulating antibodies, (Foundations Volume 2, Chapter 40A) 
serology of ocular infections, (Foundations Volume 2, Chapter 40A) 
Serologic testing, (Foundations Volume 2, Chapter 40) See also specific disease
Serologic tests
for follicular conjunctivitis, (Clinical Volume 4, Chapter 7) 
in infectious disease, (Clinical Volume 4, Chapter 1) 
for toxoplasmosis, (Clinical Volume 4, Chapter 46) 
Seronegative spondyloarthropathies, (Clinical Volume 5, Chapter 26) See also specific spondyloarthropathy
Serotonin, migraine and, (Clinical Volume 2, Chapter 16) 
Serotonin antagonists, for migraine, (Clinical Volume 2, Chapter 16) 
Serotonin antagonists/agonists, in migraine prophylaxis, (Clinical Volume 2, Chapter 16) 
Serotonin-reuptake inhibitors, in migraine prophylaxis, (Clinical Volume 2, Chapter 16) 
Serotyping, adenovirus, (Foundations Volume 2, Chapter 96) 
Serous chorioretinopathy, central. See Chorioretinopathy, central serous
Serous pigment epithelial detachments, in macular degeneration, (Clinical Volume 3, Chapter 4A) 
Serpiginous chorioretinitis, (Clinical Volume 4, Chapter 49) 
Serpiginous chorioretinopathy
indocyanine green angiography of, (Foundations Volume 2, Chapter 110A) 
Serpiginous choroiditis, (Foundations Volume 2, Chapter 113E) 
Serpiginous ulcer, chronic. See Mooren’s ulcer
Serratia, corneal ulcers from, (Clinical Volume 4, Chapter 18) 
Sertraline, for migraine, (Clinical Volume 2, Chapter 16) 
Serum, in chemical injuries, (Clinical Volume 4, Chapter 28) 
Serum alpha-fetoprotein, (Foundations Volume 3, Chapter 56) 
Serum protein binding, (Foundations Volume 3, Chapter 23) 
Serum retinol binding protein, (Foundations Volume 2, Chapter 12) 
Seton devices, complications, (Foundations Volume 3, Chapter 6) 
Seventh cranial nerve. See Facial nerve
Severe combined immunodeficiency disease (SCID), (Clinical Volume 5, Chapter 40) 
Sex
human papillomavirus and, (Foundations Volume 2, Chapter 95) 
intraocular pressure and, (Foundations Volume 2, Chapter 7) 
Sexual abuse of children, (Clinical Volume 5, Chapter 44) 
Sezolamide, (Foundations Volume 3, Chapter 30) See also Carbonic anhydrase inhibitors
dorzolamide versus, (Foundations Volume 3, Chapter 30) 
Shack-Hartman technique of aberration measurement, (Clinical Volume 1, Chapter 70) 
Shaffer grading system, (Clinical Volume 3, Chapter 44) 
Shaffer-Weiss classification of congenital glaucoma, (Clinical Volume 3, Chapter 51) 
Shagreen, crocodile, anterior mosaic, (Clinical Volume 4, Chapter 16) 
Shagreen patch, in tuberous sclerosis, 3; (Clinical Volume 5, Chapter 36) (Clinical Volume 3, Chapter 34) 
Shave biopsy, lid nevi, (Foundations Volume 3, Chapter 20) 
Sheathing, venous, in retina, Eales’ disease and, 2, (Clinical Volume 3, Chapter 16) 
Sheridan-Gardner test, (Clinical Volume 2, Chapter 2) 
Sherrington law, (Clinical Volume 1, Chapter 4) 
Shields
partial lamellar sclerouvectomy of, (Clinical Volume 4, Chapter 36) 
Shield ulcer, in vernal keratoconjunctivitis, 3, (Clinical Volume 4, Chapter 2) (Clinical Volume 4, Chapter 9) 
Shingles. See Herpes zoster
Shock, electric, cataract from, (Clinical Volume 1, Chapter 73) 
Shooting sports, eye injuries from, protective device effectiveness and, (Clinical Volume 5, Chapter 45) 
Short wavelength automated perimetry (SWAP), (Foundations Volume 2, Chapter 17) (Foundations Volume 2, Chapter 109) 
Shunts, tube. See Tube shunts
(S)-9-(3-Hydroxy-2-phosphonyl-methoxypropyl) cytosine. See HPMPC
Sialidosis, dysmorphic, (Foundations Volume 3, Chapter 54B) 
Sialidosis Type I, (Clinical Volume 5, Chapter 41) 
Sicca syndrome, (Clinical Volume 2, Chapter 35) See also Keratoconjunctivitis sicca
in cicatricial pemphigoid, treatment of, (Clinical Volume 5, Chapter 27) 
Sickle cell anemia. See also Sickle cell disease
angioid streaks and, (Clinical Volume 3, Chapter 36) 
Sickle cell disease, (Clinical Volume 3, Chapter 17 ) 
angioid streaks in, (Clinical Volume 3, Chapter 17) 
anterior segment involvement in, (Clinical Volume 3, Chapter 17) 
choroidal vascular occlusion in, (Clinical Volume 3, Chapter 17) 
clinical manifestations of, (Clinical Volume 3, Chapter 17) 
conjunctival sign of, (Clinical Volume 3, Chapter 17) 
epiretinal membranes in, (Clinical Volume 3, Chapter 17) 
laboratory evaluation of, (Clinical Volume 3, Chapter 17) 
macular small vessel occlusions in, (Clinical Volume 3, Chapter 17) 
maculopathy in, macular function testing in, (Clinical Volume 3, Chapter 17) 
pathophysiology of, (Clinical Volume 3, Chapter 17) 
posterior segment involvement in, (Clinical Volume 3, Chapter 17) 
research efforts on, (Clinical Volume 3, Chapter 17) 
retinal artery occlusion in, (Clinical Volume 3, Chapter 17) 
retinal veins in
retinopathy in, (Clinical Volume 3, Chapter 17 ) 
black sunbursts in, (Clinical Volume 3, Chapter 17) 
classification of, (Clinical Volume 3, Chapter 17) 
fundus lesions in, (Clinical Volume 3, Chapter 17) 
iridescent spots in, (Clinical Volume 3, Chapter 17) 
peripheral manifestations of, (Clinical Volume 3, Chapter 17) 
arteriolar occlusions as, (Clinical Volume 3, Chapter 17) 
arteriolar-venular anastomoses as, (Clinical Volume 3, Chapter 17) 
preretinal neovascularization as, (Clinical Volume 3, Chapter 17) 
proliferative
feeder vessel photocoagulation in, (Clinical Volume 3, Chapter 17) 
local scatter photocoagulation in, (Clinical Volume 3, Chapter 17) 
pathogenetic classification of, (Clinical Volume 3, Chapter 17) 
peripheral circumferential scatter photocoagulation in, (Clinical Volume 3, Chapter 17) 
preretinal neovascularization in, (Clinical Volume 3, Chapter 17) 
retinal detachment in, (Clinical Volume 3, Chapter 17) 
retinal hemorrhages in, (Clinical Volume 3, Chapter 17) 
vitreous hemorrhage in, (Clinical Volume 3, Chapter 17) 
thalassemia in, photocoagulation in, (Clinical Volume 6, Chapter 76) 
vascular tortuosity in, (Clinical Volume 3, Chapter 17) 
Sickle cell-hemoglobin C disease, (Clinical Volume 3, Chapter 17) 
Sickle cell retinopathy, (Foundations Volume 3, Chapter 13) 
Sickle cell-thalassemia disease, (Clinical Volume 3, Chapter 17) 
Sickle cell trait, (Clinical Volume 3, Chapter 17) 
Sickle prep test, (Clinical Volume 3, Chapter 17) 
Siderosis, foreign body, glaucoma and, (Clinical Volume 3, Chapter 54E) 
Siderosis bulbi, (Clinical Volume 4, Chapter 62) See Hemosiderosis bulbi
Siderotic glaucoma, (Clinical Volume 3, Chapter 54R) 
Siegrist streaks (spots), in hypertensive choroidopathy, (Clinical Volume 3, Chapter 13) 
Signaling pathways, conjunctival electrolyte, water transport, (Foundations Volume 2, Chapter 2) 
Signet ring carcinoma, orbital extension of, (Clinical Volume 2, Chapter 46) 
Signet ring lesion, in ocular histoplasmosis, (Clinical Volume 4, Chapter 48) 
Silastic intubation, nasolacrimal duct, (Clinical Volume 5, Chapter 79 ) 
dacryocystorhinostomy combined with, (Clinical Volume 5, Chapter 79) 
Silicone bands, in ptosis correction, (Clinical Volume 5, Chapter 88) 
Silicone expander procedure, superior oblique tendon, (Clinical Volume 6, Chapter 96) 
Silicone oil
complications of, (Clinical Volume 3, Chapter 28) 
tamponade, in acute retinal necrosis syndrome, (Clinical Volume 3, Chapter 28) 
as vitreous substitute, (Clinical Volume 6, Chapter 54)  (Clinical Volume 6, Chapter 56 ) 
in acute retinal necrosis, (Clinical Volume 6, Chapter 54) 
complications of, (Clinical Volume 6, Chapter 54) 
in cytomegalovirus retinitis, (Clinical Volume 6, Chapter 54) 
in giant retinal tears, (Clinical Volume 6, Chapter 54) 
in proliferative diabetic retinopathy, (Clinical Volume 6, Chapter 54) 
in proliferative vitreoretinopathy, (Clinical Volume 6, Chapter 54) 
in uveitis with hypotony, (Clinical Volume 6, Chapter 54) 
Silicone optic discoloration, (Clinical Volume 6, Chapter 11) 
Silicones, for lenses, (Clinical Volume 6, Chapter 11) 
Silicone tubing, for intubation of canaliculi, (Clinical Volume 4, Chapter 13) (Clinical Volume 6, Chapter 105) 
Silver nitrate
for angular blepharitis, (Foundations Volume 3, Chapter 36) 
conjunctivitis from, (Clinical Volume 4, Chapter 6) 
ocular toxicity of, (Clinical Volume 5, Chapter 37) 
in prophylaxis of neonatal conjunctivitis, (Foundations Volume 2, Chapter 64) (Foundations Volume 3, Chapter 36) 
prophylaxis with, in gonococcal ophthalmia neonatorum, (Clinical Volume 4, Chapter 6) (Clinical Volume 4, Chapter 26) 
Silver protein, ocular toxicity of, (Clinical Volume 5, Chapter 37) 
Silverstein syndrome, (Foundations Volume 3, Chapter 13) 
Simulated sheath syndrome, (Clinical Volume 1, Chapter 20) 
Simultaneous perception, (Clinical Volume 1, Chapter 5) 
Singerman-Berkow-Patz, dominant slowly progressive macular dystrophy of, (Clinical Volume 3, Chapter 9) 
Single-nucleotide polymorphism, (Foundations Volume 1, Chapter 19A) 
Sinuses
cavernous, anatomy, (Foundations Volume 1, Chapter 32) 
Sinus histiocytosis, with massive lymphadenopathy, (Clinical Volume 2, Chapter 39) 
Sinusitis. See also Paranasal sinuses; specific sinus
angle-closure glaucoma mimicking, (Clinical Volume 3, Chapter 53) 
bacterial, (Clinical Volume 5, Chapter 33) 
ethmoid, (Clinical Volume 4, Chapter 25) See also Cellulitis, orbital
classification of, 4, (Clinical Volume 4, Chapter 25) 
fungal, allergic, (Clinical Volume 2, Chapter 14) 
Sinusoidal gratings, (Foundations Volume 2, Chapter 17) 
Sinus venosus. See Schlemm’s canal
Sipple-Gorlin syndrome. See Multiple endocrine neoplasia
Sipple syndrome. See Multiple endocrine neoplasia
Sixth cranial nerve. See Abducens nerve
Sjogren-Larsson syndrome, (Clinical Volume 5, Chapter 27) 
Skeletal diseases, autosomal dominant, (Foundations Volume 3, Chapter 58) 
Skeletal disorders, (Clinical Volume 5, Chapter 29) See also specific disorders
cranial deformity syndromes and, (Clinical Volume 5, Chapter 29) 
facial deformity syndromes and, (Clinical Volume 5, Chapter 29) 
Skeletal disorders, cataracts associated with, (Clinical Volume 5, Chapter 41) 
Skeletal dysplasias, (Foundations Volume 3, Chapter 61) 
Skeleton, periorbital, embryology, (Foundations Volume 1, Chapter 3) 
Sketching of rays, (Clinical Volume 1, Chapter 30 ) 
spherical refracting surface, single
thin lens
negative
different medium on each side, (Clinical Volume 1, Chapter 30) 
same medium on each side, (Clinical Volume 1, Chapter 30) 
positive
different medium on each side, (Clinical Volume 1, Chapter 30) 
same medium on both sides, (Clinical Volume 1, Chapter 30) 
Skiing, eye injuries from, protective device effectiveness and, (Clinical Volume 5, Chapter 45) 
Skin, (Foundations Volume 3, Chapter 7)  (Foundations Volume 3, Chapter 7) 
actinic keratosis, (Foundations Volume 3, Chapter 7) 
antiseptics applied to, in postoperative prophylaxis, (Foundations Volume 2, Chapter 64) 
apocrine carcinoma, (Foundations Volume 3, Chapter 7) 
appendageal (adnexal) tumors, (Foundations Volume 3, Chapter 7) 
atypical fibroxanthoma, (Foundations Volume 3, Chapter 7) 
basal cell carcinoma, (Foundations Volume 3, Chapter 7) 
benign, premalignant, malignant tumors, (Foundations Volume 3, Chapter 7) 
cancer, (Foundations Volume 3, Chapter 7) See also Melanoma
clear cell hidradenoma, (Foundations Volume 3, Chapter 7) 
congenital abnormalities, (Foundations Volume 3, Chapter 7) 
Demodex folliculorum, (Foundations Volume 3, Chapter 7) 
dermatofibroma (histiocytoma), (Foundations Volume 3, Chapter 7) 
diseases. (See also specific disease)
gram-positive cocci in, (Foundations Volume 2, Chapter 49) 
eccrine carcinoma, (Foundations Volume 3, Chapter 7) 
eccrine spiradenoma, (Foundations Volume 3, Chapter 7) 
epidermal inclusion cysts, milia, (Foundations Volume 3, Chapter 7) 
epidermolysis bullosa, (Foundations Volume 3, Chapter 7) 
epithelial tumors, (Foundations Volume 3, Chapter 7) 
fibroepithelial papilloma (acrochordon), (Foundations Volume 3, Chapter 7) 
follicular carcinomas, (Foundations Volume 3, Chapter 7) 
follicular tumors, (Foundations Volume 3, Chapter 7) 
fungal, parasitic infections, (Foundations Volume 3, Chapter 7) 
hypersensitivity diseases. (See Hypersensitivity)
inverted follicular keratosis, (Foundations Volume 3, Chapter 7) 
lid, (Foundations Volume 1, Chapter 5) 
manifestations of systemic diseases, (Foundations Volume 3, Chapter 7) 
lid, periorbital manifestations of systemic diseases, (Foundations Volume 3, Chapter 7) 
lupus erythematosus, (Foundations Volume 3, Chapter 7) 
melanocytic nevus, (Foundations Volume 3, Chapter 7) 
melanocytic tumors, (Foundations Volume 3, Chapter 7) 
Merkel cell carcinoma, (Foundations Volume 3, Chapter 7) 
periorbital manifestations of systemic diseases, (Foundations Volume 3, Chapter 7) 
pilar (trichilemmal) cysts, (Foundations Volume 3, Chapter 7) 
pilomatrix carcinoma, (Foundations Volume 3, Chapter 7) 
Pityrosporum orbiculare, (Foundations Volume 3, Chapter 7) 
premalignant tumors, (Foundations Volume 3, Chapter 7) 
sebaceous adenoma, (Foundations Volume 3, Chapter 7) 
sebaceous carcinoma, (Foundations Volume 3, Chapter 7) 
sebaceous hyperplasia, (Foundations Volume 3, Chapter 7) 
seborrheic keratosis, (Foundations Volume 3, Chapter 7) 
squamous cell carcinoma, (Foundations Volume 3, Chapter 7) 
squamous cell carcinoma in situ, (Foundations Volume 3, Chapter 7) 
surgery, topical anesthesia, (Foundations Volume 3, Chapter 35) 
syringocystadenoma papilliferum, (Foundations Volume 3, Chapter 7) 
trichilemmal carcinoma, (Foundations Volume 3, Chapter 7) 
trichoepithelioma, (Foundations Volume 3, Chapter 7) 
trichofolliculoma, (Foundations Volume 3, Chapter 7) 
warty dyskeratoma, (Foundations Volume 3, Chapter 7) 
Skin disorders, (Clinical Volume 5, Chapter 27) See also specific disorders
acrodermatitis enteropathica as, (Clinical Volume 5, Chapter 27) 
anhidrotic ectodermal dysplasia as, (Clinical Volume 5, Chapter 27) 
in ataxia-telangiectasia, (Clinical Volume 5, Chapter 36) 
atrophic papulosis as, malignant, (Clinical Volume 5, Chapter 27) 
basal cell nevus syndrome as, (Clinical Volume 5, Chapter 27) 
in Ehlers-Danlos syndrome, (Clinical Volume 5, Chapter 27) 
in focal dermal hypoplasia syndrome, (Clinical Volume 5, Chapter 27) 
hydroa vacciniforme as, (Clinical Volume 5, Chapter 27) 
juvenile xanthogranuloma as, (Clinical Volume 5, Chapter 27) 
in Kimura’s disease, (Clinical Volume 2, Chapter 35) 
lentigines, syndrome of ocular albinism and congenital sensorineural hearing loss and, (Clinical Volume 4, Chapter 38) 
onchocerciasis and, (Clinical Volume 5, Chapter 62) 
pseudoxanthoma elasticum as, (Clinical Volume 5, Chapter 27) 
telangiectasia as, (Clinical Volume 5, Chapter 36) 
toxic epidermal necrolysis as, (Clinical Volume 5, Chapter 27) 
xeroderma pigmentosum as, (Clinical Volume 5, Chapter 27) 
Skin diving, eye injuries from, (Clinical Volume 5, Chapter 45) 
Skin flaps. See Flaps
Skin tests
in allergic conjunctivitis, (Clinical Volume 4, Chapter 2) 
in cat-scratch disease, (Clinical Volume 4, Chapter 4) 
in penicillin allergy, (Clinical Volume 4, Chapter 26) 
Slab-off grinding, of bifocals, (Clinical Volume 1, Chapter 44) 
SLE. See Lupus erythematosus
Sledding, eye injuries from, protective device effectiveness and, (Clinical Volume 5, Chapter 45) 
Sleep, therapeutic hydrogel lenses and, (Clinical Volume 4, Chapter 11) 
Sliding/rotation flaps, in lid repair, (Clinical Volume 5, Chapter 88) 
Slip knots, paracentesis and, (Clinical Volume 6, Chapter 15) 
Slipped muscle as complication of rectus muscle surgery, (Clinical Volume 6, Chapter 83) 
Slit lamp
techniques with. (See Alit lamp biomicroscopy)
Slit lamp examination, (Clinical Volume 1, Chapter 73B) 
Slit lamp ophthalmoscopy, (Clinical Volume 1, Chapter 63 ) 
for position of ocular surfaces, (Clinical Volume 1, Chapter 3) 
in scleral/episcleral disease, (Clinical Volume 4, Chapter 23) 
Slit lamp photography, in cataract, (Clinical Volume 1, Chapter 73B) 
Sloan achromatopsia test, (Foundations Volume 2, Chapter 19) 
Smallpox. See Vaccinia; Variola
Small vessel disease, (Clinical Volume 2, Chapter 19) 
Smith-Lemli-Opitz syndrome, (Clinical Volume 5, Chapter 41) 
Smith-Magenis syndrome, (Foundations Volume 3, Chapter 52) 
Smith-Magenisyndrome, (Clinical Volume 5, Chapter 41) 
Smoking. See also Tobacco
cataract risk with, (Clinical Volume 1, Chapter 72C) 
diabetic retinopathy and, (Clinical Volume 3, Chapter 30) 
Smoking, cataract with, (Clinical Volume 5, Chapter 41) 
Smoking, ocular teratogenicity, (Foundations Volume 1, Chapter 39) 
Smooth pursuit eye movements, (Foundations Volume 1, Chapter 38) 
vertical vestibular, (Foundations Volume 1, Chapter 38) 
Smooth pursuit system, (Foundations Volume 1, Chapter 38) (Foundations Volume 2, Chapter 23) 
eye movements elicited to continuously moving stimuli and, (Foundations Volume 2, Chapter 23) 
suppression of vestibulo-ocular reflex and, (Foundations Volume 2, Chapter 23) 
tracking eye movements to ramp stimuli and, (Foundations Volume 2, Chapter 23) 
vision during smooth pursuit eye movements and, (Foundations Volume 2, Chapter 23) 
Snellen diabetic retinopathy, (Clinical Volume 1, Chapter 73B) 
Snellen equivalents, (Clinical Volume 5, Chapter 51) 
Snell-Sterling visual efficiency scale, (Clinical Volume 5, Chapter 51) 
Snorkeling, eye injuries from, (Clinical Volume 5, Chapter 45) 
“Snowball” opacities, (Foundations Volume 3, Chapter 14) 
Snow banking, vitreous inflammation in, (Clinical Volume 2, Chapter 35) 
in pars planitis, (Clinical Volume 4, Chapter 43) 
Snowboarding, eye injuries from, protective device effectiveness and, (Clinical Volume 5, Chapter 45) 
"Snowflake" alteration of polymethylmethacrylate intraocular lens, (Clinical Volume 6, Chapter 11) 
Snowmobiling, eye injuries from, protective device effectiveness and, (Clinical Volume 5, Chapter 45) 
Soccer, eye injuries from, protective device effectiveness and, (Clinical Volume 5, Chapter 45) 
Social considerations, in pediatric cataract surgery, (Clinical Volume 6, Chapter 100) 
Socket
Sodium channel blockade, in glaucoma therapy, (Clinical Volume 3, Chapter 57) 
Sodium channels, visual transduction and, (Foundations Volume 2, Chapter 12) 
Sodium chloride, as hyperosmotic agent, (Foundations Volume 3, Chapter 28) 
Sodium dodecylsulfate-polyacrylamide gel electrophoresis, (Foundations Volume 2, Chapter 40) 
Sodium ethylmercurithiosalicylate. See Thimerosal
Sodium fluorescein. See Fluorescein
Sodium hyaluronate, viscoelastic material, 4–5, (Clinical Volume 6, Chapter 9) 
Sodium hydroxide, ocular injury from, (Clinical Volume 4, Chapter 28) 
Sodium perborate, cytotoxic effects, (Foundations Volume 3, Chapter 43) 
Sodium salicylate, ocular toxicity of, (Clinical Volume 5, Chapter 37) 
Soemmering ligament, (Clinical Volume 2, Chapter 40) 
Softball, eye injuries from, protective device effectiveness and, (Clinical Volume 5, Chapter 45) 
Soft contact lenses. See Contact lenses, soft
Solar maculopathy, (Clinical Volume 6, Chapter 76) 
Solar radiation. See Light toxicity
Solar retinopathy, (Clinical Volume 3, Chapter 37) 
Solid blade speculum, (Clinical Volume 6, Chapter 3) 
Solid cystic hidradenoma, (Foundations Volume 3, Chapter 7) 
Solubility
in lipids, pharmacokinetics and, (Foundations Volume 3, Chapter 23) 
of oral medications, bioinequivalence and, (Foundations Volume 3, Chapter 22) 
Solubility test, in sickle cell disease, (Clinical Volume 3, Chapter 17) 
Solu-Medrol. See Methylprednisolone
Solutions, topical, bioinequivalence and, (Foundations Volume 3, Chapter 22) 
Sommering ligaments, (Foundations Volume 1, Chapter 32) 
Soper-type keratoconus lens, (Clinical Volume 1, Chapter 54) 
Sorivudine
in herpes zoster ophthalmicus, (Clinical Volume 4, Chapter 20) 
for varicella-zoster virus, (Foundations Volume 2, Chapter 94) 
Sorsby, pseudoinflammatory macular dystrophy of. See Pseudoinflammatory macular dystrophy
Southern blot technique, genetics of lymphoma and, (Clinical Volume 2, Chapter 39) 
Spaeth angle classification system, (Clinical Volume 3, Chapter 44) 
Spaeth procedure, in telecanthus correction, (Clinical Volume 6, Chapter 110) 
Spasmus nutans syndrome, nystagmus in, (Clinical Volume 2, Chapter 11) 
Spasticity, of conjugate gaze, (Clinical Volume 2, Chapter 3) 
Spatial contrast sensitivity function, (Foundations Volume 2, Chapter 17) 
Spatial contrast sensitivity testing, (Foundations Volume 2, Chapter 17) See also Contrast sensitivity testing, spatial
Spatial discrimination, (Clinical Volume 1, Chapter 33) 
Spatial disparity. See Binocular disparity
Spatial influences, on light adaptation, (Foundations Volume 2, Chapter 16) 
Spatial information processing, (Foundations Volume 2, Chapter 13) See also Balint’s syndrome
Spatial summation, amblyopia and, (Clinical Volume 1, Chapter 10) 
color-coded ganglion cells and, (Foundations Volume 1, Chapter 20) 
Spatula, for grasping tissue, in microsurgery, (Clinical Volume 6, Chapter 3) 
Spear-shaped cataract, (Foundations Volume 1, Chapter 15) 
Specialty lenses, (Clinical Volume 1, Chapter 56) 
Specimen collection, (Foundations Volume 2, Chapter 40) 
from corneal ulcers, (Clinical Volume 4, Chapter 18) 
in orbital surgery, (Clinical Volume 5, Chapter 86) 
Spectacle, lenses, prescribing, accommodation and, (Clinical Volume 1, Chapter 36) 
Spectacle lenses, (Clinical Volume 1, Chapter 68A) (Clinical Volume 5, Chapter 47) See also Lens(es)
in amblyopia treatment, (Clinical Volume 1, Chapter 11) 
in anisometropia, (Clinical Volume 1, Chapter 33) 
correction of vertical phoria due to, (Clinical Volume 1, Chapter 44) 
athletes. (See also Sports medicine, protective devices infor)
bifocal. (See Bifocals)
binocular relationships in, (Clinical Volume 1, Chapter 36) 
changing position of, effects of, (Clinical Volume 1, Chapter 36) 
clip-on devices for, in aniseikonia corrections, (Clinical Volume 1, Chapter 47) 
clip-on devices for Fresnel prisms, (Clinical Volume 1, Chapter 52) 
cylinders in. (See Cylinder lenses)
in esotropia, accommodative, (Clinical Volume 1, Chapter 12) 
far-point plane correction with, (Clinical Volume 1, Chapter 36) 
Fresnel membrane adherence to, (Clinical Volume 1, Chapter 52) See also Fresnel optics
impact resistance of, (Clinical Volume 5, Chapter 45) 
with intraocular lenses, (Clinical Volume 1, Chapter 68) 
lensmeters. (See Lensmeters)
magnification from power (Mp), (Clinical Volume 1, Chapter 47) 
magnification in percent from its shape (Ms), (Clinical Volume 1, Chapter 47) 
multifocal, (Clinical Volume 1, Chapter 44) See also Bifocals; Trifocals
prescribing, binocularity and, (Clinical Volume 1, Chapter 36) 
press-on lenses for, (Clinical Volume 1, Chapter 52) 
retinal image size and
in axial hyperopia, (Clinical Volume 1, Chapter 33) 
in reractive ametropia, (Clinical Volume 1, Chapter 33) 
shape of, fabrication and, (Clinical Volume 1, Chapter 30) 
sunglass. (See Sunglasses)
tints and coatings for, (Clinical Volume 1, Chapter 51D ) 
total magnification of (M1), (Clinical Volume 1, Chapter 47) 
Spectinomycin, (Clinical Volume 4, Chapter 26) 
for gonococcal conjunctivitis, (Foundations Volume 3, Chapter 36) 
in gonococcal conjunctivitis, (Clinical Volume 4, Chapter 26) 
Spectral sensitivity, increment threshold, in amblyopia, (Clinical Volume 1, Chapter 10) 
Spectral sensitivity testing, (Foundations Volume 2, Chapter 14) 
Speech disorders, (Clinical Volume 5, Chapter 42) 
Speedball, eye injuries from, protective device effectiveness and, (Clinical Volume 5, Chapter 45) 
Spheno-ethmoiditis, (Clinical Volume 2, Chapter 5) 
Sphenoidal wing meningiomas, (Clinical Volume 2, Chapter 5) 
Sphenopalatine ganglion, (Clinical Volume 2, Chapter 40) 
Spherical aberrations, (Clinical Volume 1, Chapter 33) 
retinal image blur and, (Clinical Volume 1, Chapter 33) 
surgically induced, calculation of, (Clinical Volume 1, Chapter 30) 
Spherical refracting surface, (Clinical Volume 1, Chapter 20) See also Refraction
mathematical considerations on, (Clinical Volume 1, Chapter 30) 
paraxial power of, (Clinical Volume 1, Chapter 30) 
Sphincter alterations, trauma to iris and, (Clinical Volume 4, Chapter 61) 
Sphincter muscle, iris, (Foundations Volume 1, Chapter 11) 
Sphingolipidoses, perimacular retinal deposits in, (Clinical Volume 5, Chapter 30) 
Sphingomyelin lipidoses. See Niemann-Pick disease
Sphingomyelin metabolism, in Niemann-Pick disease, (Clinical Volume 3, Chapter 29) 
Spider angiomas, in pregnancy, (Clinical Volume 5, Chapter 32) 
Spider dystrophy, (Clinical Volume 3, Chapter 9) 
Spielmeyer-Sjogren disease, (Foundations Volume 3, Chapter 54B) 
Spin casting, contact lenses, (Clinical Volume 1, Chapter 55) 
Spindle cell carcinoma, (Foundations Volume 3, Chapter 8) 
Spingolipidoses, ocular changes in, (Clinical Volume 2, Chapter 5) (Clinical Volume 5, Chapter 30) 
Spinocerebellar degeneration
optic atrophy in, (Clinical Volume 2, Chapter 5) 
Spiradenoma, eccrine, (Foundations Volume 3, Chapter 7) 
Spiral valve of Hyrtl, 3, (Clinical Volume 4, Chapter 13) 
Spiramycin
for toxoplasmosis, (Clinical Volume 4, Chapter 46) 
Splenomegaly, primary, (Foundations Volume 3, Chapter 13) 
Spondylitis, ankylosing, (Foundations Volume 2, Chapter 38) See Ankylosing spondylitis
Spongium anguli iridocornealis. See Trabecular meshwork
Sporanox. See Itraconazole
Sporothrix schenckii, (Foundations Volume 3, Chapter 4) 
Sporotrichosis, conjunctival, (Clinical Volume 4, Chapter 4) 
Sports medicine. See also Athlete
equipment certification councils for, (Clinical Volume 5, Chapter 45) 
eye injuries in, (Clinical Volume 1, Chapter 56) (Clinical Volume 5, Chapter 45 ) 
all-terrain vehicles, (Clinical Volume 5, Chapter 45) 
automobile racing, (Clinical Volume 5, Chapter 45) 
classification of, (Clinical Volume 5, Chapter 45) 
equestrian sports, (Clinical Volume 5, Chapter 45) 
exercise-related, (Clinical Volume 5, Chapter 45) 
incidence of, 5–9, (Clinical Volume 5, Chapter 45) 
data gathering systems for, (Clinical Volume 5, Chapter 45) 
large ball sports, (Clinical Volume 5, Chapter 45) 
legal implications of, (Clinical Volume 5, Chapter 45) 
ocular trauma in, (Clinical Volume 5, Chapter 56) 
prevention of. (See also Sports medicine, protective devices in)
risk to individual and, (Clinical Volume 5, Chapter 45) 
risk to society and, (Clinical Volume 5, Chapter 45) 
role of eye care professionals in, (Clinical Volume 5, Chapter 45) 
visual training in, (Clinical Volume 5, Chapter 45) 
eyewear standards for, (Clinical Volume 5, Chapter 45) 
guidelines for sports participation in, (Clinical Volume 5, Chapter 45) 
prevention of, distribution of forces in, (Clinical Volume 5, Chapter 45) 
protective devices for, (Clinical Volume 3, Chapter 31) (Clinical Volume 5, Chapter 45) (Clinical Volume 5, Chapter 56) 
buying/prescribing/dispensing, (Clinical Volume 5, Chapter 45) 
classification of, (Clinical Volume 5, Chapter 45) 
equipment certification councils and, (Clinical Volume 5, Chapter 45) 
safety recommendations for, (Clinical Volume 5, Chapter 45) 
selection criteria for, (Clinical Volume 5, Chapter 45) 
Spread function in images, (Clinical Volume 1, Chapter 33) 
Spring-tension speculum, (Clinical Volume 6, Chapter 3) 
Spurious posterior polar cataract. See Mittendorf dot
Squamous blepharitis, 2, (Clinical Volume 4, Chapter 22) 
Squamous cell carcinoma, (Foundations Volume 3, Chapter 7) 
angle, gonioscopic appearance of, (Clinical Volume 3, Chapter 44) 
conjunctival
orbital extension of, (Clinical Volume 2, Chapter 46) 
ultrasound biomicroscopy, (Foundations Volume 2, Chapter 106) 
corneal, superficial keratectomy in, (Clinical Volume 6, Chapter 28) 
lid, (Clinical Volume 4, Chapter 3) 
orbital extension of, (Clinical Volume 2, Chapter 46) 
in renal transplant patients, (Clinical Volume 5, Chapter 31) 
limbal, gonioscopic appearance of, (Clinical Volume 3, Chapter 44) 
paranasal sinus, orbital extension of, (Clinical Volume 2, Chapter 46) 
in situ, epidermal, (Foundations Volume 3, Chapter 7) 
Squamous cell carcinoma in situ, (Foundations Volume 3, Chapter 7) 
Squamous metaplasia, (Foundations Volume 1, Chapter 29) 
of ocular surface, 3, (Clinical Volume 6, Chapter 34) 
Squamous papilloma, conjunctival, (Foundations Volume 3, Chapter 8) 
Squash, eye injuries from, protective device effectiveness and, (Clinical Volume 5, Chapter 45) 
SRK formula of intraocular lens power, (Clinical Volume 1, Chapter 68) 
Staining. See also specific stains
in infection diagnosis
chromogenic stains, (Foundations Volume 2, Chapter 40) 
fluorescent stains, (Foundations Volume 2, Chapter 40) 
Stains, diagnostic, (Clinical Volume 4, Chapter 1) See also specific diagnosis; specific stain
in Acanthamoeba keratitis, (Clinical Volume 4, Chapter 18A) 
in bacterial keratitis, (Clinical Volume 4, Chapter 18) 
Staircase method, in contrast sensitivity testing, (Clinical Volume 1, Chapter 35) 
Staircase procedure, in static perimetry, (Foundations Volume 2, Chapter 17) 
Stallard
trap-door approach of, (Clinical Volume 4, Chapter 36) 
Stallard procedure, in telecanthus correction, (Clinical Volume 6, Chapter 110) 
Stallard-Wright lateral orbitotomy, (Clinical Volume 5, Chapter 86) 
Stance, assessment of, in dizzy patient, (Clinical Volume 2, Chapter 18) 
Standard (full-field) electroretinography, (Clinical Volume 2, Chapter 10) 
Staphylococcal endophthalmitis, (Foundations Volume 2, Chapter 49) 
Staphylococcal scalded skin syndrome, (Foundations Volume 2, Chapter 29) 
Staphylococcal scalded skin syndrome. See Ritter’s disease
Staphylococci
bleb-related infection from, (Clinical Volume 4, Chapter 55) 
blepharitis from, (Clinical Volume 4, Chapter 22) 
corneal ulcers from, (Clinical Volume 4, Chapter 18) 
endophthalmitis caused by, (Clinical Volume 4, Chapter 55) See also Endophthalmitis
impetigo contagiosa from, (Clinical Volume 4, Chapter 22) 
in toxic epidermal necrolysis, (Clinical Volume 5, Chapter 27) 
Staphylococcus epidermidis
conjunctivitis and, (Clinical Volume 4, Chapter 5) 
as normal ocular surface inhabitant, (Clinical Volume 4, Chapter 5) 
Staphylococcus haemolyticus, (Foundations Volume 2, Chapter 49) 
Staphylococcus saprophyticus, (Foundations Volume 2, Chapter 49) 
Starburst, after radial keratotomy, (Clinical Volume 6, Chapter 41) 
Stars, magnitude of, (Clinical Volume 1, Chapter 33) 
Startle myoclonus, (Clinical Volume 2, Chapter 11) 
State of dark adaptation, (Clinical Volume 3, Chapter 6) 
Static power of eye, (Clinical Volume 1, Chapter 41) 
Stationary forms of night blindness, (Clinical Volume 3, Chapter 24) 
Statistical methods, occupational ophthalmology and, (Clinical Volume 3, Chapter 24) 
Statistics
distributions in, (Clinical Volume 5, Chapter 67) 
in field defect progression assessment, (Clinical Volume 3, Chapter 49) 
hypothesis testing in, logic of, (Clinical Volume 5, Chapter 67) 
in ophthalmic clinical research, (Clinical Volume 5, Chapter 67) See also Research, clinical
prevalence and prevalence rates in
for glaucoma defects, (Clinical Volume 5, Chapter 54) 
randomization in, (Clinical Volume 5, Chapter 67) 
sample size and related errors in, (Clinical Volume 5, Chapter 67) 
standard deviation and standard error in, (Clinical Volume 5, Chapter 67) 
type I and II errors in, (Clinical Volume 5, Chapter 67) 
STATPAC, in field defect identification, (Clinical Volume 2, Chapter 2) (Clinical Volume 3, Chapter 49) 
Status migrainosis, (Clinical Volume 2, Chapter 16) 
Steinert disease. See Myotonic dystrophy
Stellate maculopathy, Leber, (Clinical Volume 2, Chapter 5) 
Stem cells
epithelial, restoration of, in ocular surface reconstruction, (Clinical Volume 6, Chapter 34) 
limbal
deficiency of, (Clinical Volume 6, Chapter 34) See also Limbal stem cell deficiency
transplantation of, in chemical injuries, (Clinical Volume 4, Chapter 28) 
transplantation of, (Clinical Volume 6, Chapter 34) 
Stenstrom ocular measurements, (Clinical Volume 1, Chapter 33) 
Stereoacuity, tests for, (Clinical Volume 1, Chapter 5) 
in monofixation syndrome, (Clinical Volume 1, Chapter 14) 
Stereo Optical Model Optec 2000C Vision Tests, (Clinical Volume 5, Chapter 47) 
Stereopsis, (Clinical Volume 1, Chapter 5) (Clinical Volume 2, Chapter 2) (Clinical Volume 5, Chapter 47) See also Stereoacuity
distance discrimination in, (Clinical Volume 1, Chapter 33) 
intraocular lenses and, (Clinical Volume 1, Chapter 68) 
physiologic basis of, (Foundations Volume 2, Chapter 24) 
with spectacle correction in monocular aphakia, (Clinical Volume 1, Chapter 48 ) 
obstacles to binocular fusion, (Clinical Volume 1, Chapter 48) 
visual evoked potentials and, (Foundations Volume 2, Chapter 24) 
Stereopsis, neuro-ophthalmologic examination, (Clinical Volume 2, Chapter 10) 
Steric exclusion, hyaluronan and, (Foundations Volume 1, Chapter 16) 
Sterile infiltrates, corneal contact lens-associated, (Clinical Volume 4, Chapter 27) 
Sterile peripheral ulcerative keratitis, associated with collagen vascular disease, (Clinical Volume 4, Chapter 2) 
Steroid-induced glaucoma, (Clinical Volume 3, Chapter 55) 
Steroids. See Corticosteroids; Glucocorticoids; Hormones
Steroids, for central retinal vein occlusion, (Clinical Volume 3, Chapter 15) 
Steroid sulfatase deficiency, (Clinical Volume 5, Chapter 19) 
Steroid therapy. See Corticosteroid therapy
Stewart lethal midline granuloma. See Midline granuloma, lethal
Still disease. See See Arthritis, rheumatoid, juvenile; Rheumatoid arthritis, juvenile (Still’s disease)
Stimulatory antibody, (Clinical Volume 4, Chapter 34) 
hypersensitivity uveitis and, (Clinical Volume 4, Chapter 54) 
Stimulus
for automated perimetry, (Foundations Volume 2, Chapter 109) 
in perimetric testing
dynamic range of, (Clinical Volume 3, Chapter 49) 
in visual acuity evaluation, (Foundations Volume 2, Chapter 17) 
Stocker-Holt dystrophy, (Clinical Volume 4, Chapter 16) 
Storage-media antibiotics, (Foundations Volume 2, Chapter 64) 
Strabismic abnormalities, symptomatic sensory, nonparetic, 50–51
accommodative effort syndrome, 61
convergence insufficiencies, 60–61
esotropia, acquired, 57–59
acute acquired comitant estropia, 57–58
cyclic esotropia, 58–59
divergence insufficiency estropia, 58
progressive estropia with nyopia, 59
failure of fusional mechanisms, 53–57
acquired central defects, 53–55
acquired visual loss, 56–57
congenital anomalies, 55–56
problems at near, 60–61
Strabismus, (Clinical Volume 1, Chapter 8 ) 
adaptations to, (Clinical Volume 1, Chapter 8 ) 
macular versus extramacular binocular vision and, (Clinical Volume 1, Chapter 5) 
binocular vision and, (Clinical Volume 1, Chapter 8 ) 
childhood
cataract surgery and, (Clinical Volume 6, Chapter 100) 
chemodenervation in, (Clinical Volume 6, Chapter 89) 
craniofacial anomalies and, (Foundations Volume 1, Chapter 41) 
in craniostenoses, (Clinical Volume 5, Chapter 29) 
dissociated. (See Dissociated strabismus complex)
divergence paralysis in, (Clinical Volume 1, Chapter 12) 
Duane retraction syndrome and, (Clinical Volume 1, Chapter 20) 
esodeviations in, accommodative, (Clinical Volume 1, Chapter 12 ) 
esotropia in
with impaired sight, (Clinical Volume 1, Chapter 12) 
Fresnel prisms in, (Clinical Volume 1, Chapter 52) 
in Hallermann-Streiff syndrome, (Clinical Volume 5, Chapter 29) 
horizontal, chemodenervation in, (Clinical Volume 6, Chapter 89) 
incomitant, Fadenoperation for, (Clinical Volume 6, Chapter 91) 
in Marfan’s syndrome, (Clinical Volume 5, Chapter 29) 
in myasthenia gravis, (Clinical Volume 1, Chapter 20) 
ophthalmic syndromes associated with, (Foundations Volume 3, Chapter 59) 
orbital decompression and, (Clinical Volume 2, Chapter 26) 
other genetic conditions associated with, (Foundations Volume 3, Chapter 59) 
paralytic, spread of comitance in, (Clinical Volume 2, Chapter 3) 
postoperative, (Clinical Volume 2, Chapter 12) 
orbital blowout fracture and, (Clinical Volume 5, Chapter 87) 
in progressive external ophthalmoplegia, (Clinical Volume 1, Chapter 20) 
saccadic velocity measurement in, (Clinical Volume 1, Chapter 21 ) 
sensory, chemodenervation in, (Clinical Volume 6, Chapter 89) 
surgery for. (See Surgery, strabismus)
surgery in, (Clinical Volume 5, Chapter 81) (Clinical Volume 6, Chapter 83)  (Clinical Volume 6, Chapter 84) See also Surgery, of muscles
adjustable-suture, (Clinical Volume 6, Chapter 88 ) 
adjustment procedures in, (Clinical Volume 6, Chapter 88) 
complications of, (Clinical Volume 6, Chapter 88) 
contraindications to, (Clinical Volume 6, Chapter 88) 
location of adjustment in, (Clinical Volume 6, Chapter 88) 
modifications of, (Clinical Volume 6, Chapter 88) 
preferred alignment position in, (Clinical Volume 6, Chapter 88) 
preoperative preparation for, (Clinical Volume 6, Chapter 88) 
surgical technique of, (Clinical Volume 6, Chapter 88) 
timing of adjustment in, (Clinical Volume 6, Chapter 88) 
Fadenoperation in, (Clinical Volume 6, Chapter 91) 
in pediatric patient, after cataract surgery, (Clinical Volume 6, Chapter 100) 
retinal perforation during, (Clinical Volume 4, Chapter 62) 
swinging flashlight test and, (Clinical Volume 2, Chapter 2) 
in thyroid orbitopathy, (Clinical Volume 2, Chapter 36) 
vertical
chemodenervation in, (Clinical Volume 6, Chapter 89) 
in congenital fibrosis of inferior rectus muscle, (Clinical Volume 1, Chapter 20) 
Fadenoperation in, (Clinical Volume 6, Chapter 91) 
vertical deviations in, concomitant, (Clinical Volume 1, Chapter 15) 
A and V patterns in, (Clinical Volume 1, Chapter 2) (Clinical Volume 1, Chapter 6) 
V pattern in, inferior oblique muscle surgery in, (Clinical Volume 6, Chapter 87) 
Strabismus fixus convergens, acquired, (Clinical Volume 1, Chapter 20) 
Strabismus surgery, anesthesia, (Clinical Volume 6, Chapter 1) 
Stratified squamous cell mucin secretion, (Foundations Volume 2, Chapter 2) 
Stratified squamous cells, (Foundations Volume 2, Chapter 2) 
Straus needle, for retrobulbar anesthesia, (Clinical Volume 6, Chapter 1) 
Strawberry nevus, (Clinical Volume 2, Chapter 27) 
Streak retinoscopy. See Retinoscopy
Streaks, angioid. See Angioid streaks
Street hockey, eye injuries from, protective device effectiveness and, (Clinical Volume 5, Chapter 45) 
Streptococci
bleb-related infection and, (Clinical Volume 4, Chapter 55) 
blepharitis from, (Clinical Volume 4, Chapter 22) 
corneal ulcer from, (Clinical Volume 4, Chapter 18) 
endophthalmitis caused by, (Clinical Volume 4, Chapter 55) 
Streptococcus agalactiae, (Foundations Volume 2, Chapter 49) 
Streptococcus bovis, (Foundations Volume 2, Chapter 49) 
Streptococcus faecalis, (Clinical Volume 4, Chapter 18) 
Streptococcus milleri, (Foundations Volume 2, Chapter 49) 
Streptococcus pneumoniae, (Foundations Volume 2, Chapter 40A) (Foundations Volume 2, Chapter 49) 
antibiotic resistance, (Foundations Volume 2, Chapter 64) 
in cellulitis, preseptal, (Clinical Volume 4, Chapter 25) 
conjunctivitis and, (Clinical Volume 4, Chapter 5) 
as corneal pathogen, 2, (Foundations Volume 2, Chapter 42) 
Streptokiniase, in central retinal vein occlusion, (Clinical Volume 3, Chapter 15) 
Streptomyces nodosus, (Foundations Volume 2, Chapter 62) 
Streptomycin
ocular toxicity of, (Clinical Volume 5, Chapter 37) 
in oculoglandular tularemia, (Clinical Volume 4, Chapter 4) 
prophylactic, tissue transplantation and, (Foundations Volume 2, Chapter 64) 
in tuberculous blepharitis, (Clinical Volume 4, Chapter 22) 
Stretch reflex, of extraocular muscles, (Clinical Volume 1, Chapter 4) 
Striated glasses, Bagolini, (Clinical Volume 1, Chapter 9) 
in monofixation syndrome, (Clinical Volume 1, Chapter 14) 
Striate lesions, visual field defects from, (Clinical Volume 2, Chapter 7) 
Striate melanokeratosis, (Clinical Volume 4, Chapter 17) 
String of pearls, vitreous inflammation, (Clinical Volume 2, Chapter 35) 
String operation, (Clinical Volume 6, Chapter 91) 
Stroke. See Cerebrovascular disease
Stroke, ischemic, (Clinical Volume 2, Chapter 19) 
antithrombotic therapy, (Clinical Volume 2, Chapter 19) 
antithrombotic therapy in, (Clinical Volume 2, Chapter 19) 
aortic arch atherosclerotic disease, (Clinical Volume 2, Chapter 19) 
blocking excitotoxic influences, (Clinical Volume 2, Chapter 19) 
evaluation of causes, (Clinical Volume 2, Chapter 19) 
ischemic penumbra, increasing collateral flow to, (Clinical Volume 2, Chapter 19) 
large vessel disease, (Clinical Volume 2, Chapter 19) 
large vessel manifestations, (Clinical Volume 2, Chapter 19) 
small vessel disease, (Clinical Volume 2, Chapter 19) 
small vessel manifestations, (Clinical Volume 2, Chapter 19) 
transient ischemic attacks, (Clinical Volume 2, Chapter 19) 
vascular risk factors, (Clinical Volume 2, Chapter 19) 
Stroma, (Foundations Volume 1, Chapter 8) 
glycosaminoglycans, (Foundations Volume 1, Chapter 8) 
lamellar organization, (Foundations Volume 1, Chapter 8) 
uveal, embryology, (Foundations Volume 1, Chapter 2) 
Stromal ingrowth, (Foundations Volume 3, Chapter 19) 
after cataract extraction, (Foundations Volume 3, Chapter 6) 
Structural folds of Schwalbe, (Foundations Volume 1, Chapter 11) 
Sturge-Weber syndrome (encephalotrigeminal angiomatosis), (Foundations Volume 3, Chapter 58) 
ocular manifestations, (Foundations Volume 3, Chapter 58) 
systemic manifestations, (Foundations Volume 3, Chapter 58) 
Stye. See Hordeolum
Stye, in staphylococcal lid infection, (Clinical Volume 4, Chapter 22) 
Subacute gangliosidosis, (Foundations Volume 3, Chapter 54B) 
Subcapsular cataract. See Cataract, subcapsular
Subconjuctival chemoreduction, in retinoblastoma, (Clinical Volume 6, Chapter 109) 
Subconjunctival hemorrhage, (Foundations Volume 3, Chapter 8) 
Subfoveal membranes, surgical removal of, (Clinical Volume 6, Chapter 62 ) 
Suborbicularis fascia, (Clinical Volume 2, Chapter 21) 
Subpigment epithelial masses, lymphoma and, (Clinical Volume 5, Chapter 23) 
Subretinal fibrosis, diffuse, (Clinical Volume 4, Chapter 49) 
Subretinal fluid
drainage of
complications during, (Clinical Volume 6, Chapter 59) 
in scleral buckling, (Clinical Volume 6, Chapter 59) 
management of, in scleral buckling
nondrainage procedures in, (Clinical Volume 6, Chapter 59) 
Subretinal hemorrhage. See Hemorrhage, subretinal
Subretinal neovascular membranes, in ocular histoplasmosis, (Clinical Volume 4, Chapter 48) 
Subretinal proliferation in proliferative vitreoretinopathy, surgical removal of strands in, (Clinical Volume 6, Chapter 62) 
Subsensitivity
adrenergic transmitters and, (Foundations Volume 3, Chapter 29) 
cholinergic receptors and, (Foundations Volume 3, Chapter 26) 
Substance P
in nonspecific “reflex” keratouveitis, (Clinical Volume 4, Chapter 39) 
receptors for, blockage of, in herpes zoster treatment, (Clinical Volume 4, Chapter 20) 
Substantia propria, (Foundations Volume 1, Chapter 29) 
Succinylcholine
intraoperative dosage and administration of, for children, (Clinical Volume 6, Chapter 81) 
ocular toxicity of, (Clinical Volume 5, Chapter 37) 
Succinylcholine (Anectine)
anticholinesterase agents and, (Foundations Volume 3, Chapter 43) 
intraocular pressure affected by, (Foundations Volume 2, Chapter 7) 
Suction cup, in outflow measurement, (Foundations Volume 2, Chapter 7) 
Sugar-induced cataracts, (Clinical Volume 1, Chapter 71) 
Sugars, cataract and, (Foundations Volume 2, Chapter 10) 
Sulcus
orbital, superior, (Foundations Volume 1, Chapter 5) 
superior eyelid, defect in, surgical management of, (Clinical Volume 5, Chapter 83) 
Sulcus posterior chamber lens (unsutured), (Clinical Volume 6, Chapter 8) 
Sulfacetamide
in angular blepharitis, (Foundations Volume 3, Chapter 36) 
in conjunctivitis and keratitis, (Foundations Volume 3, Chapter 39) 
systemic toxicity of, (Clinical Volume 5, Chapter 37) 
Sulfamethizole, systemic toxicity of, (Clinical Volume 5, Chapter 37) 
Sulfamethoxazole. See Trimethoprim-sulfamethoxazole (TMP/SMX)
Sulfatide lipidosis (metachromatic leukodystrophy), (Foundations Volume 3, Chapter 13) (Foundations Volume 3, Chapter 54B) 
Sulfatidosis, juvenile, (Foundations Volume 3, Chapter 13) 
Sulfisoxazole, systemic toxicity of, (Clinical Volume 5, Chapter 37) 
Sulfites, side effects, in infants and children, (Foundations Volume 3, Chapter 43) 
Sulfur hexafluoride, (Clinical Volume 6, Chapter 81) 
as vitreous substitute, (Clinical Volume 6, Chapter 56) 
Sulindac. See Nonsteroidal anti-inflammatory drugs (NSAIDs)
Sulindac, ocular toxicity of, (Clinical Volume 5, Chapter 37) 
Sumatriptan, for migraine, (Clinical Volume 2, Chapter 16) 
Sunbursts, black, in sickle cell retinopathy, (Clinical Volume 3, Chapter 17) 
Sunglasses, (Clinical Volume 3, Chapter 24) 
labeling requirements for, (Clinical Volume 5, Chapter 55) 
lens shape and contour of, (Clinical Volume 5, Chapter 55) 
Sunlight, (Foundations Volume 2, Chapter 15) See also Ultraviolet radiation; See also Light toxicity; Ultraviolet radiation
xeroderma pigmentosum and, (Clinical Volume 5, Chapter 27) 
Sunset syndrome, sulcus-fixated PC IOL and, (Clinical Volume 6, Chapter 8) 
Superficial basal cell carcinoma, (Foundations Volume 3, Chapter 7) 
Superficial blood supply for eyelid, (Clinical Volume 5, Chapter 72) 
Superficial choroiditis, Holthouse-Batten, (Clinical Volume 3, Chapter 9) 
Superficial corneal neovascularization, contact lens-associated, (Clinical Volume 4, Chapter 27) 
Superficial keratectomy. See Keratectomy, superficial
Superficial keratitis, (Clinical Volume 4, Chapter 17) 
Superficial keratopathy. See Keratopathy, superficial
Superficial punctate keratitis, (Clinical Volume 4, Chapter 17) 
Superior anterior obitotomies, (Clinical Volume 5, Chapter 86) 
upper eyelid crease approach, (Clinical Volume 5, Chapter 86) 
vertical-lid-split superior orbitotomy, (Clinical Volume 5, Chapter 86) 
Superior colliculus. See Colliculus, superior
Superior eyelid sulcus defect, surgical management of, (Clinical Volume 5, Chapter 83) 
Superior limbic keratoconjunctivitis, (Foundations Volume 3, Chapter 8) (Foundations Volume 3, Chapter 9) 
filamentary keratitis with, (Clinical Volume 4, Chapter 17) 
Superior oblique muscle, (Foundations Volume 1, Chapter 1) See Oblique muscles, superior
Superior oblique tendon
in Brown syndrome, (Clinical Volume 1, Chapter 20) 
surgical trauma to, (Clinical Volume 1, Chapter 20) 
tenotomy of, in Brown syndrome, (Clinical Volume 1, Chapter 20) 
Superior ophthalmic vein. See Ophthalmic vein, superior
Superior orbital fissure, (Foundations Volume 1, Chapter 32) 
Superior orbital fissure inflammatory syndrome. See Tolosa-Hunt syndrome
Superior orbital sulcus, (Foundations Volume 1, Chapter 5) 
Superior orbitotomy. See also Orbitotomy
vertical lid split, (Clinical Volume 5, Chapter 86) 
Superior quadrantanopia, (Clinical Volume 2, Chapter 7) 
Superior sulcus deformity, (Clinical Volume 5, Chapter 82) 
Superior tarsal muscle, (Foundations Volume 1, Chapter 5) 
Superior vena cava syndrome, glaucoma and, (Clinical Volume 3, Chapter 54E) 
Supernumerary chromosome 22q, (Foundations Volume 3, Chapter 52) 
Superoanterior orbitotomy, (Clinical Volume 5, Chapter 86) See also Orbitotomy
Superotemporal branch retinal vein obstruction, (Foundations Volume 2, Chapter 113C) 
Superotemporal vein, (Foundations Volume 1, Chapter 1) 
Supersensitivity
Adie’s syndrome and, (Foundations Volume 3, Chapter 26) 
to catecholamines, (Foundations Volume 3, Chapter 29) 
topical phenylephrine and, (Foundations Volume 3, Chapter 29) 
cholinergic receptors and, (Foundations Volume 3, Chapter 26) 
Suppression hypothesis, (Foundations Volume 2, Chapter 24) 
Suppression scotoma, in esotropia and exotropia, (Clinical Volume 1, Chapter 9) 
Suppressor/cytotoxic T cells, (Clinical Volume 4, Chapter 2) 
Suprachoroidal hemorrhage, (Clinical Volume 6, Chapter 15) 
Suprachoroidal space, (Foundations Volume 1, Chapter 1) 
Supramolecular organization of vitreous, (Clinical Volume 3, Chapter 38) 
Supranuclear disorders of eye movements, (Clinical Volume 2, Chapter 10) 
brainstem saccade circuits, (Clinical Volume 2, Chapter 10) 
cerebellar influences, (Clinical Volume 2, Chapter 10) 
cerebellar lesions, (Clinical Volume 2, Chapter 10) 
vascular syndromes of cerebellum, (Clinical Volume 2, Chapter 10) 
cerebral, basal ganglionic control, (Clinical Volume 2, Chapter 10) 
gaze, functional disturbances of, (Clinical Volume 2, Chapter 10) 
horizontal gaze, (Clinical Volume 2, Chapter 10) 
effects of lesions of pons, medulla on horizontal gaze, (Clinical Volume 2, Chapter 10) 
motor commands for conjugate (versional) horizontal movements, (Clinical Volume 2, Chapter 10) 
Huntington’s disease, (Clinical Volume 2, Chapter 10) 
ocular motor apraxia, (Clinical Volume 2, Chapter 10) 
Parkinsonian disorders, (Clinical Volume 2, Chapter 10) 
saccade generation, (Clinical Volume 2, Chapter 10) 
saccades, roles for, (Clinical Volume 2, Chapter 10) 
superior colliculus, (Clinical Volume 2, Chapter 10) 
unilateral hemispheric lesions, disturbances of gaze with, (Clinical Volume 2, Chapter 10) 
vergence eye movements, (Clinical Volume 2, Chapter 10) 
disorders of vergence, (Clinical Volume 2, Chapter 10) 
divergence paresis, paralysis, (Clinical Volume 2, Chapter 10) 
spasm of near reflex, (Clinical Volume 2, Chapter 10) 
vertical, torsional movements, (Clinical Volume 2, Chapter 10) 
dorsal midbrain syndrome, (Clinical Volume 2, Chapter 10) 
midbrain lesions, (Clinical Volume 2, Chapter 10) 
vertical deviations, sustained, (Clinical Volume 2, Chapter 10) 
vestibulo-ocular system, (Clinical Volume 2, Chapter 10) 
Supranuclear palsy, progressive, (Clinical Volume 2, Chapter 10) 
Supranuclear pathway, (Clinical Volume 2, Chapter 8) 
eyelid opening disorders and, (Clinical Volume 2, Chapter 8) 
Supraorbital artery, (Foundations Volume 1, Chapter 5) 
Supraorbital foramen, (Foundations Volume 1, Chapter 32) 
Supraorbital nerve, (Foundations Volume 1, Chapter 5) 
Supraorbital sinuses, (Foundations Volume 1, Chapter 32) 
Supraorbital vein, (Foundations Volume 1, Chapter 5) 
Suprathreshold static perimetry, (Foundations Volume 2, Chapter 17) 
Supratrochlear artery, (Foundations Volume 1, Chapter 5) 
Suprofen. See Nonsteroidal anti-inflammatory drugs (NSAIDs)
Surface ablation, (Clinical Volume 6, Chapter 48) 
clinical results, (Clinical Volume 6, Chapter 48) 
preoperative evaluation, (Clinical Volume 6, Chapter 48) 
surgical technique, (Clinical Volume 6, Chapter 48) 
Surface dyslexia, (Clinical Volume 2, Chapter 7) 
Surface tension, tear film, (Foundations Volume 2, Chapter 3) 
Surface wrinkling retinopathy. See Epiretinal membranes
Surfactants, topical, bioinequivalence and, (Foundations Volume 3, Chapter 22) 
Surfing, eye injuries from, protective device effectiveness and, (Clinical Volume 5, Chapter 45) 
Surgery. See also See also Anesthetics; Microsurgery and specific operation; Surgical complications; Wound healing; specific procedures
for Acanthamoeba keratitis, (Clinical Volume 4, Chapter 18A) 
in Acanthamoeba keratitis, (Foundations Volume 2, Chapter 80) 
anesthesia in. (See Anesthesia)
in anophthalmic socket, (Clinical Volume 5, Chapter 83 ) 
anterior segment, after radial keratotomy, (Clinical Volume 6, Chapter 41) 
arc of contact in, (Clinical Volume 6, Chapter 91) 
aseptic technique in, in endophthalmitis prevention, (Clinical Volume 4, Chapter 24) 
in astigmatism correction, (Clinical Volume 6, Chapter 42) See also Keratotomy, astigmatic
after penetrating keratoplasty, (Clinical Volume 6, Chapter 26) 
bleeding complications in, thrombocytopenia and, (Clinical Volume 5, Chapter 23) 
brow, telecanthus and, (Clinical Volume 6, Chapter 110) 
for canthal dystopia, in craniofacial syndromes, (Clinical Volume 6, Chapter 110) 
cataract, (Clinical Volume 6, Chapter 6) See also Cataract, surgery
cellulitis after, orbital, (Clinical Volume 4, Chapter 25) 
in children
for corneal opacities, (Clinical Volume 6, Chapter 106 ) 
discharge criteria after, (Clinical Volume 6, Chapter 81) 
intraoperative concerns in, (Clinical Volume 6, Chapter 81) 
choroidal neovascular membrane excision, (Clinical Volume 6, Chapter 62L) 
in Coats’ disease, (Clinical Volume 6, Chapter 72) 
complications of, (Clinical Volume 6, Chapter 84) 
for congenital fibrosis of inferior rectus muscle, (Clinical Volume 1, Chapter 20) 
conjunctival, complications, (Foundations Volume 3, Chapter 8) 
corneal
corneal power change induced by, calculation of, (Clinical Volume 1, Chapter 30) 
corticosteroids and, postoperative NSAIDs and, (Foundations Volume 3, Chapter 38) 
in craniofacial anomalies, (Foundations Volume 1, Chapter 41) 
in craniofacial syndromes, (Clinical Volume 6, Chapter 110 ) 
in craniopharyngioma, (Clinical Volume 2, Chapter 6) 
for dissociated strabismus complex, (Clinical Volume 1, Chapter 18) 
endophthalmitis after, 2, (Clinical Volume 4, Chapter 24) 
enucleation. (See Enucleation)
epiretinal macular membrane removal, (Clinical Volume 6, Chapter 61) 
for esotropia, (Clinical Volume 6, Chapter 84) 
with impaired sight, (Clinical Volume 1, Chapter 12) 
nonaccommodative, acquired, (Clinical Volume 6, Chapter 84) 
operative considerations for, (Clinical Volume 6, Chapter 84) 
postoperative considerations on, (Clinical Volume 6, Chapter 84) 
preoperative considerations for, (Clinical Volume 6, Chapter 84) 
sixth nerve palsy in, (Clinical Volume 6, Chapter 84) 
A and V patterns and, (Clinical Volume 6, Chapter 84) 
exenteration, (Clinical Volume 5, Chapter 83) See also Exenteration
for exotropia, reoperation, (Clinical Volume 6, Chapter 98) 
extraocular muscles. (See Surgery, of musclesof)
eyebrow, telecanthus and, (Clinical Volume 6, Chapter 110) 
of eyelids, (Clinical Volume 5, Chapter 78 ) 
blepharoplasty as. (See Blepharoplasty)
in craniofacial syndromes, (Clinical Volume 6, Chapter 110) 
in Graves’ disease, (Clinical Volume 2, Chapter 14) 
in horizontal lid laxity repair, (Clinical Volume 5, Chapter 74) 
in lacrimal drainage system disorders, (Clinical Volume 4, Chapter 13) (Clinical Volume 5, Chapter 79) 
reconstructive, (Clinical Volume 5, Chapter 42) See also Reconstructive surgery, of eyelids
for foreign body removal, (Clinical Volume 6, Chapter 66) 
frontal sinus, simulated sheath syndrome and, (Clinical Volume 1, Chapter 20) 
in generalized fibrosis syndrome, (Clinical Volume 1, Chapter 20) 
for glare disability, (Clinical Volume 1, Chapter 31) 
glaucoma. (See Glaucoma, surgery)
globe compression during, ischemic optic neuropathy due to, (Clinical Volume 2, Chapter 5) 
in herpes simplex keratitis, (Clinical Volume 4, Chapter 19) 
in human papillomavirus, (Foundations Volume 2, Chapter 95) 
infection during, potential sources of, (Clinical Volume 4, Chapter 24) 
of inferior oblique muscles, (Clinical Volume 6, Chapter 87 ) 
anterior transposition of, (Clinical Volume 6, Chapter 87) 
in dissociated vertical deviations, (Clinical Volume 1, Chapter 18) 
complications of, (Clinical Volume 6, Chapter 87) 
contraindications to, (Clinical Volume 6, Chapter 87) 
dissociated vertical deviations and, (Clinical Volume 6, Chapter 87) 
preferred techniques for, (Clinical Volume 6, Chapter 87) 
in primary inferior oblique overaction, (Clinical Volume 6, Chapter 87) 
in secondary inferior oblique overaction, (Clinical Volume 6, Chapter 87) 
weakening of, in Duane’s syndrome, (Clinical Volume 6, Chapter 96) 
intracapsular, anesthesia for, (Clinical Volume 6, Chapter 1) 
in iridocyclitis, chronic, (Clinical Volume 4, Chapter 42) 
iridocyclitis after, (Clinical Volume 4, Chapter 62) 
ischemic optic neuropathy after, (Clinical Volume 2, Chapter 5) 
of lacrimal drainage system, (Clinical Volume 4, Chapter 13)  (Clinical Volume 5, Chapter 79 ) 
in acquired problems, (Clinical Volume 5, Chapter 79 ) 
in congenital abnormalities, (Clinical Volume 5, Chapter 79) 
in congenital obstruction, (Clinical Volume 4, Chapter 13) (Clinical Volume 6, Chapter 105 ) 
dacryocystorhinostomy in, (Clinical Volume 6, Chapter 105) 
silicone tube intubation in, (Clinical Volume 6, Chapter 105) 
in lower system blocks, (Clinical Volume 5, Chapter 79) 
reconstruction of, after tumor excision, (Clinical Volume 5, Chapter 79) 
in upper system blocks, (Clinical Volume 5, Chapter 79) 
in lacrimal gland tumors, (Clinical Volume 2, Chapter 40) 
lasers in. (See Laser(s); specific procedure)
in melanoma, posterior uveal, (Clinical Volume 6, Chapter 70 ) 
local resection in, (Clinical Volume 6, Chapter 70) 
complications of, (Clinical Volume 6, Chapter 70) 
relative indications for, (Clinical Volume 6, Chapter 70) 
miosis in
inhibition, NSAIDs in, (Foundations Volume 3, Chapter 38) 
muscarinic agonists in, (Foundations Volume 3, Chapter 26) 
of muscles
for anomalous head positions, postoperative, (Clinical Volume 6, Chapter 98) 
in craniofacial syndromes, (Clinical Volume 6, Chapter 110) 
in exotropia, reoperation, (Clinical Volume 6, Chapter 98) 
in Graves’ disease, (Clinical Volume 2, Chapter 36) 
inferior oblique, (Clinical Volume 6, Chapter 87) See also Surgery, of inferior oblique muscles
levator, technique of, (Clinical Volume 6, Chapter 104) 
myotomy. (See Myotomy)
rectus, (Clinical Volume 6, Chapter 83) See also Surgery, of rectus muscles
reoperation, (Clinical Volume 6, Chapter 98 ) 
for anomalous head positions, (Clinical Volume 6, Chapter 98) 
complications of, (Clinical Volume 6, Chapter 98) 
contraindications to, (Clinical Volume 6, Chapter 98) 
nonincisional (chemosurgery), (Clinical Volume 6, Chapter 98) 
nonsurgical interventions and, (Clinical Volume 6, Chapter 98) 
preoperative considerations on, (Clinical Volume 6, Chapter 98) 
for vertical deviations, (Clinical Volume 6, Chapter 98) 
superior oblique. (See Surgery, of superior oblique muscles)
in thyroid orbitopathy, (Clinical Volume 2, Chapter 36) 
transposition as
horizontal, of vertical rectus muscles, (Clinical Volume 6, Chapter 97) 
saccadic velocity and, (Clinical Volume 1, Chapter 21) 
vertical rectus muscle, (Clinical Volume 6, Chapter 96) 
in myopia, (Clinical Volume 4, Chapter 66) See also Radial keratotomy
epikeratoplasty as, (Clinical Volume 6, Chapter 45) 
keratomileusis as, (Clinical Volume 6, Chapter 46 ) 
normal wound healing and, (Foundations Volume 3, Chapter 6 ) 
of oblique muscles
inferior oblique weakening procedures as, (Clinical Volume 1, Chapter 17) (Clinical Volume 6, Chapter 87) 
superior oblique weakening procedures as, (Clinical Volume 1, Chapter 17) 
oculoplastic, anesthesia for, (Clinical Volume 6, Chapter 1) 
in optic gliomas, (Clinical Volume 2, Chapter 42) 
orbital, (Clinical Volume 2, Chapter 14)  (Clinical Volume 5, Chapter 86 ) 
anatomic considerations on, (Clinical Volume 2, Chapter 14) 
complications of, (Clinical Volume 2, Chapter 14) 
for foreign body removal, (Clinical Volume 5, Chapter 87) 
in Graves’ disease, (Clinical Volume 2, Chapter 14) 
hemostasis during, (Clinical Volume 5, Chapter 86) 
in idiopathic intracranial hypertension, (Clinical Volume 2, Chapter 14) 
imaging before, 3, (Clinical Volume 5, Chapter 86) 
instrumentation for, (Clinical Volume 5, Chapter 86) 
intraoperative considerations in, (Clinical Volume 5, Chapter 86) 
orbitotomy as, (Clinical Volume 5, Chapter 86) See also Orbitotomy
lateral, for pleomorphic adenoma, (Clinical Volume 2, Chapter 40) 
patient history and, (Clinical Volume 5, Chapter 86) 
physical examination before, (Clinical Volume 5, Chapter 86) 
postoperative management of, (Clinical Volume 2, Chapter 14) 
specimen handling for, (Clinical Volume 5, Chapter 86) 
in traumatic optic neuropathy, (Clinical Volume 2, Chapter 14) 
patient position for, retinochoroidal infarction and, (Clinical Volume 2, Chapter 5) 
phacoemulsification, (Clinical Volume 6, Chapter 7) See also Phacoemulsification
physical preparation for, in children, (Clinical Volume 6, Chapter 80 ) 
pituitary, in adenoma, (Clinical Volume 2, Chapter 6) 
posterior fixation procedure as, (Clinical Volume 6, Chapter 91) 
postoperative care for, in children, cataract surgery and, (Clinical Volume 6, Chapter 100) 
postoperative concerns in, for children
postoperative conditions after
blindness as, (Clinical Volume 2, Chapter 5) 
after reoperation of extraocular muscles, (Clinical Volume 6, Chapter 98) 
in children
intraocular lens implantation and, (Clinical Volume 6, Chapter 101) 
penetrating keratoplasty and, (Clinical Volume 6, Chapter 106) 
cystoid macular edema as, (Clinical Volume 4, Chapter 55) 
dacryocystorhinostomy and, (Clinical Volume 5, Chapter 79) 
early bacterial endophthalmitis as, (Clinical Volume 4, Chapter 55)  (Clinical Volume 6, Chapter 64) 
epikeratophakia and, (Clinical Volume 6, Chapter 103) 
eyelid trauma and, (Clinical Volume 5, Chapter 75 ) 
fungal endophthalmitis as, (Clinical Volume 4, Chapter 55) 
graft rejection as, (Clinical Volume 6, Chapter 26) 
Irvine-Gass syndrome as, (Clinical Volume 4, Chapter 55) 
keratomileusis and, (Clinical Volume 6, Chapter 46) 
noninfectious uveitis as, (Clinical Volume 4, Chapter 55) 
penetrating keratoplasty and, (Clinical Volume 6, Chapter 26) 
postoperative period
antimicrobial prophylaxis, (Foundations Volume 2, Chapter 64 ) 
postponement of, in children, (Clinical Volume 6, Chapter 80) 
preoperative evaluation and preparation for
in blepharoplasty, (Clinical Volume 5, Chapter 74) 
endophthalmitis prevention and, (Clinical Volume 4, Chapter 24) 
in epikeratophakia, (Clinical Volume 6, Chapter 103) 
in esotropia surgery, (Clinical Volume 6, Chapter 84) 
in foreign body removal, (Clinical Volume 6, Chapter 66) 
in keratomileusis, (Clinical Volume 6, Chapter 46) 
in lacerating anterior segment trauma, (Clinical Volume 6, Chapter 39) 
in orbital surgery, (Clinical Volume 5, Chapter 86) 
in reoperation of extraocular muscles, (Clinical Volume 6, Chapter 98) 
in strabismus surgery, adjustable-suture, (Clinical Volume 6, Chapter 88) 
in proliferative vitreoretinopathy, (Clinical Volume 6, Chapter 56) 
in pseudotumor cerebri, (Clinical Volume 2, Chapter 5) 
psychological preparation for, in children, (Clinical Volume 6, Chapter 80) 
ptosis, (Clinical Volume 5, Chapter 72) See also Ptosis, surgery for
radial keratotomy and, (Clinical Volume 6, Chapter 41) 
of rectus muscles, (Clinical Volume 6, Chapter 83 ) 
in Duane’s syndrome, (Clinical Volume 6, Chapter 96 ) 
Fadenoperation in, (Clinical Volume 6, Chapter 91 ) 
posterior fixation suture for, (Clinical Volume 6, Chapter 96) 
recession procedure in
in Duane’s syndrome, (Clinical Volume 6, Chapter 96) 
Fadenoperation and, (Clinical Volume 6, Chapter 91) 
lateral rectus muscle in, (Clinical Volume 6, Chapter 96) 
medial rectus muscle in, (Clinical Volume 6, Chapter 96) 
transposition as. (See Surgery, of muscles, transposition as)
vertical rectus weakening as, (Clinical Volume 6, Chapter 96) 
Y-splitting procedure as, 5, (Clinical Volume 6, Chapter 96) 
refractive
contact lens fitting after, (Clinical Volume 1, Chapter 54) 
corneal edema and, (Clinical Volume 4, Chapter 16A) 
custom, wavefront technology in, (Clinical Volume 1, Chapter 70) 
epikeratoplasty as, (Clinical Volume 6, Chapter 45 ) 
glare sensitivity after, (Clinical Volume 1, Chapter 35) 
keratomileusis as, (Clinical Volume 6, Chapter 46 ) 
keratotomy as
myopia correction and, (Clinical Volume 1, Chapter 42) 
specialty lenses after, (Clinical Volume 1, Chapter 56) 
retinal detachment, (Foundations Volume 3, Chapter 13) 
color Doppler imaging after, (Foundations Volume 2, Chapter 102) 
for retinoblastoma, (Clinical Volume 6, Chapter 109) 
retroequatorial myopexy as, (Clinical Volume 6, Chapter 91) 
scleral buckling after, glaucoma and, (Clinical Volume 3, Chapter 54E) 
scleral buckling and, (Clinical Volume 6, Chapter 59) 
in sickle cell retinopathy, (Clinical Volume 3, Chapter 17) 
Silastic intubation of nasolacrimal duct and, (Clinical Volume 5, Chapter 79) 
slipped muscles in, (Clinical Volume 1, Chapter 20) 
sports activity after, (Clinical Volume 5, Chapter 56) 
strabismus, (Foundations Volume 2, Chapter 23) 
arc of contact and, (Foundations Volume 2, Chapter 23) 
bilateral elevation or depression of muscle insertions and, (Foundations Volume 2, Chapter 23) 
effect of antagonist and, (Foundations Volume 2, Chapter 23) 
elevation of medial rectus and depression of lateral rectus insertion and, (Foundations Volume 2, Chapter 23) 
elevation of muscle insertions and, (Foundations Volume 2, Chapter 23) 
oblique muscle transpositions and, (Foundations Volume 2, Chapter 23) 
for strabismus, (Clinical Volume 6, Chapter 83) See also Surgery, for esotropia; Surgery, of inferior oblique muscles; Surgery, of rectus muscles; Surgery, of superior oblique muscles
adjustable-suture, (Clinical Volume 6, Chapter 88 ) 
angioid streaks and, (Clinical Volume 3, Chapter 36) 
for pathologic myopia, (Clinical Volume 3, Chapter 36) 
retinal perforation during, (Clinical Volume 4, Chapter 62) 
strabismus after, (Clinical Volume 2, Chapter 12) 
subfoveal membrane removal in, (Clinical Volume 6, Chapter 62 ) 
subfoveal membrane removal and, (Clinical Volume 6, Chapter 62) 
subretinal, in histoplasmosis, (Clinical Volume 4, Chapter 48) 
of superior oblique muscles, (Clinical Volume 6, Chapter 86 ) 
surgeon performing, patient’s knowledge of, ethical considerations on, (Clinical Volume 5, Chapter 68) 
sympathetic ophthalmia and, (Clinical Volume 4, Chapter 55L) 
Third World countries, (Clinical Volume 5, Chapter 58) See also Third World countries, ophthalmology inin
in thyrotoxicosis ophthalmoplegia, (Clinical Volume 1, Chapter 20) 
timing of, children and, (Clinical Volume 6, Chapter 80) 
torsional, contraindications to, (Clinical Volume 6, Chapter 97) 
trauma caused by, (Clinical Volume 1, Chapter 20) 
unnecessary, right t to, (Clinical Volume 5, Chapter 68) 
in uveitis, (Clinical Volume 4, Chapter 54) (Clinical Volume 4, Chapter 64 ) 
band keratopathy, (Clinical Volume 4, Chapter 64) 
for cataract extraction, (Clinical Volume 4, Chapter 64 ) 
cyclitic membrane in, (Clinical Volume 4, Chapter 64) 
Fuch’s heterochromic cyclitis in, (Clinical Volume 4, Chapter 64) 
general approach to, (Clinical Volume 4, Chapter 64) 
inflammatory membrane over surface of lens and connected to iris, (Clinical Volume 4, Chapter 64) 
iris management in, (Clinical Volume 4, Chapter 64) 
juvenile rheumatoid arthritis and iridocyclitis in, (Clinical Volume 4, Chapter 64) 
lens-induced uveitis and, (Clinical Volume 4, Chapter 64) 
pars planitis in, (Clinical Volume 4, Chapter 64) 
special problems in, (Clinical Volume 4, Chapter 64) 
vitreous cells and opacities in, (Clinical Volume 4, Chapter 64) 
general measures for, (Clinical Volume 4, Chapter 64) 
surgical sampling in, (Clinical Volume 4, Chapter 35) 
uveitis following. (See Uveitis, postoperative)
in vernal keratoconjunctivitis, (Clinical Volume 4, Chapter 9) 
vitreoretinal
corneal edema and, (Clinical Volume 4, Chapter 16A) 
for posterior segment trauma, (Clinical Volume 6, Chapter 66 ) 
vitreous. (See also Vitrectomy)
anatomic considerations on, (Clinical Volume 6, Chapter 51 ) 
microsurgery
for foreign body removal, (Clinical Volume 6, Chapter 66) 
for secondary repair after trauma treatment, (Clinical Volume 6, Chapter 66) 
in proliferative vitreoretinopathy, (Clinical Volume 6, Chapter 56) 
in A and V patterns, (Clinical Volume 6, Chapter 84) 
in xerophthalmia, (Clinical Volume 5, Chapter 59) 
Surgical complications, (Foundations Volume 3, Chapter 6 ) 
of antiglaucoma surgery, (Foundations Volume 3, Chapter 6) 
of glaucoma surgery, ultrasound biomicroscopy, (Foundations Volume 2, Chapter 106) 
of penetrating keratoplasty, (Foundations Volume 3, Chapter 6) 
postoperative infections, (Foundations Volume 3, Chapter 12) 
antimicrobial prophylaxis and, (Foundations Volume 2, Chapter 64 ) 
of refractive surgery, (Foundations Volume 3, Chapter 6) 
of retinal detachment and vitreous surgery
vitreous adhesions, (Foundations Volume 3, Chapter 14) 
Surgical limbus, healing, (Foundations Volume 3, Chapter 6) 
Surveillance, in ophthalmic epidemiology, (Foundations Volume 2, Chapter 43) 
Surveys, in ophthalmic epidemiology, (Foundations Volume 2, Chapter 43) 
Suspensions, topical, bioinequivalence and, (Foundations Volume 3, Chapter 22) 
Sus’ruta, history of anesthesia, (Clinical Volume 6, Chapter 1) 
Sustentacular cell, in paraganglioma, (Clinical Volume 2, Chapter 41) 
Sutures, (Clinical Volume 1, Chapter 71A) (Clinical Volume 6, Chapter 15) 
adjustable, in strabismus surgery, (Clinical Volume 6, Chapter 88 ) 
argon laser lysis, (Clinical Volume 6, Chapter 19) 
biofilm development around, (Foundations Volume 2, Chapter 52) 
in cataract surgery, in pediatric patient, (Clinical Volume 6, Chapter 100) 
compression, in astigmatic keratotomy, (Clinical Volume 6, Chapter 42) 
erosion of, in secondary IOL implantation, (Clinical Volume 6, Chapter 8) 
in intraocular lens fixation, (Clinical Volume 6, Chapter 26) 
laser lysis, after filtration surgery, (Clinical Volume 1, Chapter 69B) (Clinical Volume 6, Chapter 24) 
lens, development as function of age, (Clinical Volume 1, Chapter 71B) See also Lens sutures
needle types for, (Clinical Volume 6, Chapter 3) 
in penetrating keratoplasty, (Clinical Volume 6, Chapter 26) 
removal of, in children, (Clinical Volume 6, Chapter 106) 
posterior fixation
in dissociated vertical deviations, (Clinical Volume 1, Chapter 18) 
in Duane’s syndrome, (Clinical Volume 6, Chapter 96) 
removal and cutting, antimicrobial prophylaxis for, (Foundations Volume 2, Chapter 64) 
scleral
explant technique for, (Clinical Volume 6, Chapter 59) 
Fadenoperation and, 6–7, (Clinical Volume 6, Chapter 91) 
traction, (Clinical Volume 6, Chapter 3) 
in parabulbar (subTenon’s) anesthesia, (Clinical Volume 6, Chapter 1) 
transsclerally sulcus-sutures PC IOL implantation, (Clinical Volume 6, Chapter 8) 
SWAP (short wavelength automated perimetry), (Foundations Volume 2, Chapter 17) (Foundations Volume 2, Chapter 109) 
Swedish interactive threshold algorithm, in automated perimetry, (Clinical Volume 3, Chapter 49) 
Swimming, eye injuries from, protective device effectiveness and, (Clinical Volume 5, Chapter 45) 
Swinging flashlight test, in relative afferent pupillary defect, (Clinical Volume 2, Chapter 2) (Clinical Volume 2, Chapter 15) 
Symblepharon
in chemical injuries, (Clinical Volume 4, Chapter 28) 
in erythema multiforme, (Clinical Volume 5, Chapter 27) 
Symblepharon. See Cryptophthalmos
Symbolic agnosia, (Clinical Volume 2, Chapter 4) 
Symmetric fixation, horopter with, (Foundations Volume 2, Chapter 24) 
Sympathetic nerves
pupillary
excitation, and darkness reflex, (Foundations Volume 2, Chapter 9) 
Sympathetic nerves, stimulation of protein secretion by, (Foundations Volume 2, Chapter 2A) 
Sympathetic nerve supply, eyelid anatomy and, (Clinical Volume 5, Chapter 72) 
Sympathetic ophthalmia, (Clinical Volume 4, Chapter 40) (Clinical Volume 4, Chapter 51)  (Clinical Volume 4, Chapter 54) (Clinical Volume 4, Chapter 51) (Clinical Volume 4, Chapter 55) 
after vitrectomy, (Clinical Volume 6, Chapter 56) 
clinical manifestations, (Clinical Volume 4, Chapter 51) 
cytotoxic antibody in, (Clinical Volume 4, Chapter 34) 
histopathology of, (Clinical Volume 4, Chapter 51) 
iridocyclitis and, (Clinical Volume 4, Chapter 42) 
pharmaceutical agents, (Clinical Volume 4, Chapter 51) 
Sympathetic ophthalmia. See Ophthalmia, sympathetic; Uveitis, sympathetic
Sympathetic pathways, ocular, defects in, (Clinical Volume 2, Chapter 29) See also Horner’s syndrome
Sympathomimetics
intraocular pressure and, (Foundations Volume 2, Chapter 7) 
systemic toxicity of, (Clinical Volume 5, Chapter 37) 
Synaptic connections, retinal, (Clinical Volume 3, Chapter 1) 
Synaptic transmission, optic nerve and, (Foundations Volume 2, Chapter 21) 
Syndromes associated with altered lens geometry, (Clinical Volume 5, Chapter 41) 
Synechiae
anterior, in uveitis, (Clinical Volume 4, Chapter 32) 
cataract extraction in uveitis and, (Clinical Volume 4, Chapter 64) 
cataract surgery and, pediatric, (Clinical Volume 6, Chapter 100) 
central posterior, 2, (Clinical Volume 3, Chapter 54D) 
indirect-acting muscarinic agonists in, (Foundations Volume 3, Chapter 26) 
peripheral anterior, (Clinical Volume 3, Chapter 54D) 
ultrasound biomicroscopy, (Foundations Volume 2, Chapter 106) 
posterior
after cataract extraction, (Foundations Volume 3, Chapter 6) 
angle-closure glaucoma due to, (Foundations Volume 3, Chapter 19) 
in juvenile rheumatoid arthritis, 3, (Clinical Volume 4, Chapter 42) 
in posterior polymorphous dystrophy, (Clinical Volume 3, Chapter 61) 
Synergism
of corticosteroids and NSAIDs, (Foundations Volume 3, Chapter 38) 
Synergy hypothesis, (Foundations Volume 2, Chapter 24) 
Synkineses, of facial nerve, (Foundations Volume 1, Chapter 37) 
jaw-winking. (See Marcus Gunn phenomenon)
“near, ”, (2) 15: 6
Synkinetic near response, (Clinical Volume 1, Chapter 7) 
horizontal fusion vergence and, (Clinical Volume 1, Chapter 7) 
Syphilis, (Clinical Volume 4, Chapter 50)  (Clinical Volume 4, Chapter 57) (Clinical Volume 5, Chapter 33) (Clinical Volume 5, Chapter 40) See also Treponema pallidum; (Foundations Volume 2, Chapter 32) (Foundations Volume 2, Chapter 70) 
Argyll Robertson pupil in, (Clinical Volume 2, Chapter 15) 
cardiovascular manifestations of, (Foundations Volume 2, Chapter 70) 
clinical manifestations of, (Clinical Volume 5, Chapter 33) 
global prevalence of, (Foundations Volume 2, Chapter 70) 
human immunodeficiency virus and, (Foundations Volume 2, Chapter 70) 
interstitial keratitis in, (Clinical Volume 4, Chapter 58) 
iridocyclitis in, (Clinical Volume 4, Chapter 42) 
keratitis caused by, (Foundations Volume 2, Chapter 70) 
laboratory diagnosis of, (Foundations Volume 2, Chapter 70) 
ocular complications, (Foundations Volume 3, Chapter 4) 
ocular involvement in, (Clinical Volume 5, Chapter 33) 
ocular manifestations of, (Foundations Volume 2, Chapter 70) 
optic nerves in, (Clinical Volume 2, Chapter 5) 
pathophysiology of, (Foundations Volume 2, Chapter 70) 
polymerase chain reaction diagnosis of, (Foundations Volume 2, Chapter 70) 
Syringocystadenoma papillerum, (Foundations Volume 3, Chapter 7) 
Syringocystadenoma papilliferum, (Foundations Volume 3, Chapter 7) 
Syringocystadenoma papilliferum, of lid, (Clinical Volume 4, Chapter 3) 
Systemic arterial hypertension, fluorescein angiography, (Foundations Volume 2, Chapter 113C) 
Systemic diseases. See also specific disease
cataracts in, (Clinical Volume 1, Chapter 73)  (Clinical Volume 5, Chapter 41) See also under Cataract
chromosomal disorders and. (See Chromosome abnormalities)
cornea in, (Clinical Volume 4, Chapter 15 ) 
furrow degeneration in, (Clinical Volume 4, Chapter 16) 
problem solving in, (Clinical Volume 4, Chapter 15) 
hematologic. (See Hematologic disorders)
infectious and inflammatory, (Clinical Volume 5, Chapter 33) See also Infection; Inflammation
metabolic. (See metabolic disorders)
orbital disease and, (Clinical Volume 2, Chapter 35) 
thyroid, management of, (Clinical Volume 2, Chapter 36) 
Systemic diseases, cataract from, (Clinical Volume 1, Chapter 73) 
Systemic fibrosclerosis, (Clinical Volume 2, Chapter 35) 
Systemic infection, cataract associated with, (Clinical Volume 5, Chapter 41) 
Systemic lupus erythematosus. See Lupus erythematosus
Systemic sclerosis, progressive. See Scleroderma
Systemic therapy, pharmacokinetics and, (Foundations Volume 3, Chapter 23) 
Systemic xanthogranulomatosis, (Clinical Volume 2, Chapter 35) 
Systolic click-murmur syndrome. See Mitral valve prolapse

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