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Index

A

A17 amacrine cells, branching cells, 82

A18 amacrine cells, wide-field amacrine, 82 Abducens damage, 230b–231b

Abducens nerve, 188 cranial nerve VI, 227 pathway, 227 sagittal section, 225f

Abducens nucleus, 227 Accessory lacrimal glands

contribution, 177 presence, 171f

secretory cell groups, 170–171 Accessory lacrimal glands of Wolfring, 165 Accommodation, 53b

loss (presbyopia), 55b

Accommodation-convergence reaction (near-point reaction), 260–261

Acetylcholine, presence, 27 Actin

insolubility, 101 myofibrils, 183f

myosin junction, breakage, 183 Actin filaments, sets, 182

Action potential, impact, 6

Active transport mechanisms, energy usage, 6–7 Adenosine triphosphate (ATP), myosin attachment, 182 Adie pupil OD, 267f

Adie tonic pupil, 266b Adrenergic agonists, actions, 260f

Adrenergic antagonists, actions, 261f

Adrenergic neuromuscular junction, adrenergic agonist actions, 260f Adult lens, 98f

cortex, 98f

optical section, 100f structure, determination, 93

Aerobic glycolysis, ATP yield, 7 Afferent pathway, 218–224

accommodation-convergence reaction, 261 disruption, 262–265

indication, 264f

Afferent pupillary defect, 265b

Afferent pupillary light pathway, visual pathway (parallelism), 262 Against-the-rule astigmatism, occurrence, 10b

Age-related cataracts, 104f Age-related cortical cataract, 105

Age-related macular degeneration (AMD), 57b changes, 59

presence, 58f

Age-related nuclear cataract (ARNC), 105–106 Age-related vitreal changes, 119–120

Aging changes, 35b

clinical manifestations, 103 Agonist muscles, 195–197 Agonists (drugs), 259–260 AII cell (amacrine cell), 69

All-trans-retinal isomer, formation, 80 Altered macrophages, 40

Amacrine cells, 69 AII cell, 69

whole-mount view, 70f cell body, 69

ganglion cells, differentiation, 131 information, horizontal direction, 81–82 relays, 81f

synaptic contacts, 74f types, description, 69

Amacrines, glycine/GABA release, 78–79 Amorphous ground substance, components, 6 Anatomic directions, 2–4, 3f

Anatomic planes, 2–4, 3f

Anchoring collagen fibrils, branching/anastomosing network, 12 Anisocoria, 267b, 269f

Anisotropic band (A band), 182

Annular muscle of Müller, incompletion, 135 Annulus of Zinn (common tendinous ring), 153, 185

rectus muscles, origin, 226f Antagonist muscles, 195–197 Antagonists (drugs), 259–260 Anterior (anatomic direction), 3 Anterior border layer, iris, 40 Anterior chamber, 109–111, 137–138

aging chambers, 116–117 aqueous exit, 97

circumference, trabecular meshwork (impact), 109 light micrograph, 41f

lining, 138

Anterior chamber angle inclusion, 41f structure, 97f, 109–111

importance, 99b

transverse section, light micrograph, 111f

Anterior choriocapillaris, ciliary muscle (relationship), 206f Anterior ciliary arteries, 207–209

branches, 209f branching, 207–209

rectus muscles, relationship, 206f Anterior ciliary veins, 215

fluid absorption, 97

Anterior corneal surface, curvature, 21 Anterior epithelium, 42

basal aspect, myofilaments (proliferation), 137 continuation, 42

Anterior eye, vitreous relationships, 117f Anterior gamma suture, 98f

Anterior iris

apical epithelial portion, 45f basal muscular portion, 45f contraction folds, 43 epithelial layers, position, 43 epithelium, portions, 45f surface, 43

Anterior ischemic optic neuropathy, 205b

Page references followed by “f” indicate figure, by “b” indicate box, and by “t” indicate table.

273

274 Index

Anterior knees of Wilbrand, 241 Anterior lens capsule

light micrograph, 95f thickness, 94f

Anterior lens epithelium, light micrograph, 95f, 97f Anterior limbal boundary, Descemet’s membrane

(tapering), 33 Anterior scleral foramen, 32

Anterior segment, periphery, 110f Anterior stroma, light micrograph, 15f Anterior synechia, occurrence, 43b

Anterior zonular insertion, scanning electron micrograph, 100f

Antiangiogenic factor, production, 75–76 Aponeurosis, 167

extensions, 163 Apoptosis, occurrence, 138

Aquaporin channel proteins, changes, 104 Aquaporins (AQPs), 6–7, 23–24 Aqueous chambers, 109

Aqueous dynamics, 96–97 Aqueous function, 56 Aqueous humor, 1

flow, 98f

metabolites/oxygen/glucose, provision, 97 Aqueous outflow

apparatus/tissues, drawing, 95f impedance, PAS (impact), 43b system, 110f

Aqueous production, 55–56 age-related decrease, 117

ciliary body capillaries/epithelial layers, impact, 55 circadian rhythm, relationship, 56

rate, 56

Arcuate scotoma, automated visual field, 247f Argyll Robertson pupil

left eye, 266f

light-near dissociation, 265 right eye, 266f

Arteries, radial branches, 46f Arterioles, formation, 134 Ascorbate, impact, 104

Astigmatism (clinical comment), 10b Astrocytes, 70

Automated visual field

arcuate scotoma/nasal step, 247f congruent defects, 248f

Autonomic efferent pathway, 253 Autonomic fibers, ganglion exit, 256 Autonomic nervous system, flow chart, 254f

Autonomic neurotransmitters, action sites, 259f Autonomic pathway, 253–258

Autonomic responses (alteration), pharmacologic agents (impact), 258

Axenfeld, scleral nerve loops, 220b Axons, 6

myelination, 138

B

Basal cells

keratin filaments, connection, 11–12 migration, 12

polygonal shape, 14f Basal lamina, 11

Bruch membrane, 53 Basement membrane

impact, 45f interruption, 53, 55f

material, deposit (excess), 57 RPE, 53

Basement membranelike strip, interposition, 51f Basilar artery, vertebral branches, 236 Basolateral membrane, ions (exit), 55–56

Bays processes, 49f Benign anisocoria, 267b

Bergmeister’s papilla, 130b, 131f

Best’s disease, right fundus (photo), 77f Beta proteins, stabilization, 100–101 Biomicroscope

examination, 174b usage, 4–5

Biomolecules, impact, 101

Bipolar axons, IPL termination, 80–81 Bipolar cells, 66–67

dendrites, plasma membrane, 80 information, transfer, 81 migration, 131

neural signal, 68 second-order neuron, 66 synaptic contacts, 74f

Bipolar dendrites synapse, 72 Bipolar terminals, contact, 73f Bitemporal visual field loss, 248f Blepharitis, 171b Blood-aqueous barrier, 56–57 Blood-retinal barrier, 88

Blood supply, 199 increase, 209b

innervation, relationship, 198–199 Blood vessels

absence, 99 importance, 28

fundus view, 88b permeability/barriers, 140–141

Blood vessels, sympathetic innervation, 234f Blow-out fracture, mechanism, 152f

Blue cone bipolar cell synapses, 67 Blunt trauma, 40b

Body structures, tissues, 5 Bowman’s layer, 13–15, 26

appearance, 135 characteristics, 13–15 corneal nerve, passage, 14f degeneration, 35b emergence, 136f junctions, 11

prenatal production, 15 regeneration, absence, 26

removal, photorefractive keratoplasty (usage), 15 sensory nerves, passage, 27

termination, 32–33, 110f Brain

information processing, occurrence, 218 lateral view, 125f

sagittal section, 224f, 226f Brodmann areas, 239f Brown’s syndrome, 198f

Brown superior oblique sheath syndrome, 197b Bruch membrane (basal lamina), 53

presence, 54f Bruch’s membrane

choroid section, 61

collagenous zones, basement membrane material deposit (excess), 57

development, 135

elastic sheet, presence, 135 layers, 55f

lipid accumulation, implications (summary), 58f

Brush bipolars, 66–67 Bulbar conjunctiva

biomicroscopic examination, 174b coverage, 172

fornices, 167 stretching, absence, 159 translucency, 173

Index 275

C

Cadherins, 7–8

Calcarine fissure, 243–244 visual pathway, 239f

Calcium ion channels, vesicle fusion facilitation, 78 Canaliculi, 178

tubes, 178

Canal of Hannover, 111 Canal of Petit, 111

Canal of Schlemm, 50f, 110–111 inclusion, 41f

lumen, presence, 31f

Capillaries, peripapillary network, 88 Capillary beds, formation, 134 Capillary blood flow, measurement, 83 Capillary networks, formation, 87 Capillary system, 206f

Capsulopalpebral fascia (lower eyelid aponeurosis), 163 Carbonic anhydrase inhibitors, usage, 116 Carotid-cavernous sinus fistula, 215b

Carotid plexus, fibers, 253 Cataracts, 103–106

afferent pupillary defect, 265b clinical cataracts, 103b–104b formation, 103

physiology, 104–106 surgery, 104b

Cation channels, 6–7 closure, 80

Caudal (anatomic direction), 3 Cavernous sinus, 215–216

coronal section, 215f cross section, 223f thrombosis, 215b

wall, trochlear nerve (entry), 227 Cell adhesion molecules (CAMs), 7 Cell body, 64

Cell cords, palisade periphery, 34 Cell division, cessation, 127 Cell membrane

composition, 6 fluid/solute transport, 6–7 outer leaflet, contact, 7

surface, ridge-like elevations (fusion), 7 Cell migration, requirement, 26

Cell mitosis, location, 94–95

Cell size, coefficient of variation (determination), 22f Cells/rods (outer segments), relationship (3D drawing),

63f

Cell stability, 7–8

Cell-to-matrix adhesion, control, 26 Cellular anterior border layer, 41f

Cellular cytoplasm (cytosol), protein fibers (presence), 6 Cellular metabolic functions, 7

Cellular organelles, 99

Cell volume, regulation, 102

Central cornea, corneal nerve damage, 27–28 Central foveal reflex, 85b

Central human retina, ganglion cells, 68f Central meniscus of Kuhnt, 235f

Central nervous system (CNS), disruption, 265 Central retina, 83–86

Central retinal artery, 202–204, 214 branch, 202

Central vessels, atrophy, 137 Cerebral cortex, medial surface, 239f

Cerebral hemisphere, optic radiations (location), 244f Chalazion, 171b

photograph, 172f

Characteristic visual field defects, 246b Chemical-gated stimulants, 6–7 Chemical synapses, 78

Chlorine (Cl-) flux, importance, 102

Cholesterol molecules, impact, 6 Cholinergic agonists, actions, 261f Cholinergic antagonists, actions, 261f Cholinergic neuromuscular junction, 261f Chondroitin/dermatan sulphate (CS/DS), 16 Choriocapillaris, 53

basement membrane, interruption, 53, 55f density/diameter, reduction, 59 fenestration, 88

function, maintenance, 75–76 network, 54f

Choroid, 40, 51–53, 135 aging changes, 59

blood supply, drawing, 54f Bruch’s membrane, 61 extension, 51–52 functions, 57

innervation, 54f layers, histology, 52f

posterior termination, 235f stroma

characteristics, 52–53 melanocytes, 52

tissue, absence, 128f vessels, innervation, 53

Choroidal blood supply, drawing, 54f

Choroidal blood vessels, parasympathetic innervation, 237–238

Choroidal fissure, 124 Choroidal stroma, 52–53

characteristics, 52–53 Choroidal tissue, absence, 128f Choroidal vessels

blood flow, 210 evidence, 88f innervation, 53

Chromatic aberration, reduction, 83 Chromophore, photon absorption, 79 Cilia (cilium), 64

abnormalities, 161b

hair follicle, light micrograph, 171f Ciliary artery, branch, 202

Ciliary body, 40, 135 aging changes, 58

capillaries, aqueous production/secretion, 55 components, 50f

division, 47 epithelial layers, 61 functions, 53–57 inclusion, 41f inner aspect, 49f

light micrograph, 51f longitudinal muscle, 97f muscle, 50f partitions/layers, 48f section, 209f supraciliaris, 48

transverse section, light micrograph, 50f zonule fibers, 47–48

Ciliary epithelial layers, light micrograph, 52f Ciliary epithelium (ciliary epithelia), 51

layers, light micrograph, 52f

production (inhibition), drugs (usage), 116 Ciliary ganglion, 188

characteristics, 255–256 damage, 266

Ciliary junction, 30b Ciliary muscle, 48

components, 50f

connective tissue, increase, 58 contraction, 98

impact, 53b inhibition, 256b

276

Index

 

 

 

 

 

 

 

 

Ciliary muscle (Continued)

Cones (Continued)

 

innervation, 48

pedicle, 66f

 

longitudinal fibers, contraction, 53b

electron micrograph, 73f

 

parasympathetic innervation, 255f

population

 

presence, 50f

discrimination, 76–77

 

relaxation, 99

increase, 133

 

Ciliary nerve

synapses, 66f

 

choroidal entry, 54f

Confluent drusen, 58f

 

location, 256

Congenital cataract, 128b

 

Ciliary processes

Congenital Horner syndrome, iris heterochromia, 268f

 

anterior view, 49f

Congruent defects, automated visual field, 248f

 

stroma, fenestrated capillary network, 55

Conjunctiva, 172–175

 

Ciliary stroma, 48–49

blood vessels, 174

 

pressure, estimation, 55

cysts/concretions, 169b

 

Cilioretinal artery, 205b

deep fibrous layer, connection, 169

 

retina entry, 88

epithelium, light micrograph, 168f

 

Circadian rhythm, 83

formation, 139

 

aqueous production, relationship, 56

fornix, 172

 

light/dark cycle, 83

innervation, 174–175

 

wake/sleep cycle, 83

loops, impact, 29f

 

Circle of iris, 206f

lymphatics, 174

 

Circle of Willis, optic chiasm (relationship), 236f

partitions, 174f

 

Circle of Zinn, 204

stromal vessels, presence, 31f, 110f

 

formation, 135

submucosa, initiation, 33

 

Circular furrows, iris, 49f

Conjunctivitis, 175b

 

Circular receptive field, 82

Connecting stalk, 64

 

Claudin, 7

Connective tissue, 5–6

 

Clinical aging changes, 35b

circular band, 153

 

Clinical cataracts, 103b–104b

derivation, 139

 

Cloquet’s canal, 118

fibers, components, 5–6

 

formation, 138

septa, 190

 

Closed eye conditions, oxygen supply, 24

muscle connection, 190

 

Clump cells, 40

sheath, 234

 

Coats (tunics), 1

sleeves/pulleys (identification), MRI (usage), 190

 

Cocaine

 

system

 

impact, 259–260

cross section, anterior orbit, 191f

 

test, 269f

cross section, midorbit, 191f

 

Coefficient of variation (CV) determination, 22f

Connexins

 

Collagen, 118–119

proteins, combination, 8–9

 

bands, sclera, 52

Contact lenses

 

fibers, 5–6

effects, 21b

 

fibrils, 176

wear affect, 165b

 

formation, dysfunction, 25

Contraction, initiation, 259

 

inner core, 109–110

Contralateral hemifield, 244b–245b

 

separation, 5–6

Contralateral inferior nasal retinal fibers, 241–242

 

Collagen fibrils

Conventional outflow pathway, 97–98

 

arrangement, 18

Cornea, 10–29, 134–135

 

characteristics, 15–16

appearance, 10

 

latticework, 15–16

aqueous humor, refractive index (change), 21

 

orientation, 17f

arcus, 35b

 

theoretic orientation, 17f

white limbal band, 35f

 

Collector channels, 97f

avascularity, immune privilege creation, 28

 

Coloboma, 127b

blood supply, 28–29

 

keyhole appearance, 128f

branches, radiation, 220

 

Color vision, area (occupation), 83–84

central region, development, 136f

 

Columnar basal cells, light micrograph, 15f

collagen fibrils, theoretic orientation, 17f

 

Common tendinous ring (annulus

columnar basal cells, light micrograph, 15f

 

of Zinn), 153

curvature, impact, 4

 

Cones, 65–66

deep cornea, three-dimensional drawing, 20f

 

bipolar cells, camera lucida drawings, 67f

deturgescence, 22–23

 

body, 64

dimensions, 10

 

cilium, 64

radius/view/sagittal section, 11f

 

composition, 64

dystrophy (keratoconus), 18b

 

distribution, 78f

edema, 25b–26b

 

inner fiber, 64

endothelial cells, ion/water movement (depiction), 25f

 

inner segment, 64

endothelium, 18–21

 

shape, 65–66

aging changes, 35b

 

morphology, 64–66

epithelium, abrasion, 25b–26b

 

outer fiber, 64

erosion

 

outer segment, 64

age-related changes, 13b

 

membranous discs, 65f

pain, 13b

 

renewal, 65

recurrence, 13b

 

shortness, 65

fibroblasts (keratocytes), characteristics, 16

Index 277

Cornea (Continued)

Corneal epithelium (Continued)

function, 21–27

surface layer, 10–11

histologic features, 10–21

three-dimensional drawing, 14f

hydration, 22–24

tissue, repair, 12

innermost layer, 18

turnover time, 12

innervation, 27–28, 220f

Corneal neovascularization, 28b

density, 27

Corneal reflex, 256b

lamellae, arrangement, 16

Corneal reshaping, 29b

layers

Corneal sensitivity, assessment, 28b

light micrograph, 13f

Corneal sensory innervation, 218–220

presence, 135

Corneal stroma, precursor, 136f

visualization, 5

Corneal surface

light micrograph, 167f

curvature map, corneal topography (usage), 12f

light transmission, 21–22

evaluation, 12b

metabolic activity, glucose/oxygen (impact), 24

maintenance, 12

metabolism, 24–26

Corneal touch reflex, 259f

middle layer, characteristics, 15

Corneoscleral junction, 32

neovascularization, 28b

Corneoscleral meshwork, 97f, 109

nerves

Corneoscleral trabecular sheets, 114f

Bowman’s layer passage, 14f, 15

Corona ciliaris (pars plicata), 47

damage, 27–28

Coronal (anatomic plane), 3

overnight swelling, 25b

Coronal sections, 249f

oxygen

Corrugator superciliaris, 159

derivation, 24

Cortex

supply, reduction, 25

composite drawing, 96f

physiological aging changes, 35

lens fibers, light micrograph, 97f

puncture, 15f

thickness, 98–99

refractive power, curvature (impact), 4

zones, divisions, 96

removal, 100f

Cortical cataract, 103b–104b

repair, wound healing, 26–27

spokes, visibility, 105f

reshaping, 29b

Cortical regions, activity, 238

restructuring methods, enhancement, 29b

Cortical subcapsular changes, 104f

sensitivity, assessment, 28b

Cranial (anatomic direction), 3

sensory innervation, 27

Cranial cavity (posterior floor), formation, 144

shape, 10

Cranial nerve damage, 228b

squamous surface cells, light micrograph, 15f

Cranial nerve III (oculomotor nerve), 224–225

stimulation, 27

sagittal section, 226f

stroma, 15–18

Cranial nerve IV (trochlear nerve), 225–227

precursor, 136f

sagittal section, 226f

summary diagram, 17f

Cranial nerve VI

views, 16f

abducens nerve, 227

substantia propria, 15–18

sagittal section, 226f

superficial cells, junction (scanning electron micrograph), 13f

Cranial nerve VII, facial nerve, 227–231

surface cells, age/degeneration, 11

Cranium

sympathetic nerve fibers, presence, 27

bones, 144

thickness

venous sinus drainage, superior view, 216f

impact, 21

Cribiform layer, 110–111

reduction, clinical effects, 29b

Cribiform plate, 148

topography, 12f

Crossed retinal ganglion cell axons, course, 243f

touch reflex, 259f

Crypts, 43

transparency, blood vessels (absence), 28

Crypts of Henle, 168

water, movement, 23

Crystalline lens

wavelength absorption, 102

accommodation, 97–99

wing cells, light micrograph, 15f

aging

wound healing, 26–27

changes, 102–106

Corneal arcus, 35b

clinical manifestations, 103

white limbal band, 35f

capsule, 93–94

Corneal edema, 25b–26b

transparency, 93–94

Corneal endothelium

composite drawing, 96f

aging changes, 35b

curvature, 98–99

continuity, 95f

development, protein manufacture, 100–101

formation, 134–135

dimensions, 93

Corneal epithelium, 10–12

divisions, 96

acetylcholine, presence, 27

elliptic structure, 93

basal cell layer

embryologic development, 93

columnar cells, 11

epithelium, 94–95

mitosis, occurrence, 26

fiber interface, 95–96

cells

glucose, collection, 101

ion/water movement, depiction, 24f

histology, 93–96

layers, display, 14f

ionic current, schematic, 102f

light micrograph, 15f

location, 2

middle layer, wing cells, 11

metabolism, 101

replacement, 12–13

physiology, 99–102

278

Index

 

 

 

 

 

 

 

 

Crystalline lens (Continued)

Dry eye, 177b

 

slit-lamp appearance, 99b

Ductions, 184–185

 

sutures, 96–97

eye movements, 185f

 

vascular supply, absence, 95

Ducts of Wolfring glands, characteristics, 170–171

 

Crystalline lens fibers, 95

Dura mater, periosteal layer, 155

 

components, 100–101

E

 

cytoplasm, protein concentration, 95

 

formation, 101

Early neovascularization, conjunctival loops (impact), 11f

 

production, continuation, 95

Ectoderm, impact, 123

 

Crystallins, 95

Ectropion, 162b

 

aggregation, 100–101

Edinger-Westphal nucleus, efferent parasympathetic

 

Cuneus gyrus, projections, 243–244

pathway, 262

 

Cup-to-disc ratios, variability, 87f

Effector sites, neurotransmitter (binding), 259

 

Cyclorotations, 184–185

Efferent fibers, 218

 

Cytoplasmic cGMP

Efferent parasympathetic pathway, 262

 

concentration, 79

Efferent pathway, 224–231

 

decrease, occurrence, 80

disruption, 266

 

Cytoplasmic filaments, hairpin loops, 7–8

Elastic fibers, 5–6

 

Cytoskeleton

coverage, 109–110

 

filaments, 7

Electron dense bar, extension, 78

 

structure, control, 26

Electroretinogram (ERG), 78b

 

Cytosol, protein fibers (presence), 6

11-cis-retinol, re-isomerization, 80

 

D

 

Embryo

 

 

eye, light micrograph, 139f

 

Damaged muscle, determination, 197b

eye, section, 137f, 139f

 

Dapiprazole, adrenergic antagonist, 260

hyaloid arterial system, light micrograph, 129f

 

Dark adaptation, 82–83

lens placode, thickening, 129f

 

Dark current, 79

orbit, 139f

 

Deep cornea

Embryo, dorsal surface, 124f

 

nerves, abundance, 220f

Embryonic fissure, 124

 

three-dimensional drawing, 20f

Embryonic nucleus, development, 94f

 

Dense connective tissue, 5

illustration, 129f

 

Dentate processes, 49f

Embryonic plate, formation, 123

 

Depolarizing bipolar cells (DBCs), 80

Emmetropia, 4f

 

Descemet’s membrane, 18, 26

light rays, focus, 4

 

basement membrane, consideration, 18

Emmetropization, 138b

 

corneal innermost layer, adjacency, 16

Endoderm, impact, 123

 

damage, 26

Endoplasmic reticulum (ER) network, 6

 

endothelium, basement membrane, 18

Endothelial cell

 

evidence, 134–135

basal surface indentation (formation), 97–98

 

laminae, presence, 18

giant vacuoles, formation, 100f

 

layers, attachment, 18

Endothelial covering, loss, 110

 

tapering, 33

Endothelial function, loss (Fuchs’ dystrophy), 24b

 

termination, 31f, 32–33, 109

impact, 25b–26b

 

thickness

Endothelium, 18–21, 24

 

change, age (impact), 19f

basement membrane, 18

 

increase, 35

cells

 

Descemet’s stripping automated endothelial keratoplasty (DSAEK), 28b

density, 20

 

Desmosome, 7–8

polyhedral characteristic, 18

 

appearance, 135

cell-to-cell contact, 20

 

Desmosome-like attachments, 72

energy stores, requirement, 25

 

Developing lens, presence (importance), 138

fluids/solutes, leakage, 24

 

Dextroversion, 185

Fuchs endothelial dystrophy, 23f

 

Diabetic cataract, glucose (impact), 104–105

integrity (evaluation), coefficient of variation

 

Diffuse cone bipolar cells, types, 66–67

(determination), 22f

 

Dilation lag, 269f

metabolic function, maintenance, 25

 

Dilator muscle, 42

mitosis, occurrence (absence), 27

 

presence, 42, 46f

mosaic, 21f

 

termination, 42

water movement, 24

 

Disc components, radiolabeled amino acids pulse (application), 65

Energy-utilizing ion pumps, 22–23

 

Disciform scarring, 58f

Entropion, 162b

 

Disc margins, flatness, 87

Epicanthus, 161b

 

Discontinuity, zones, 103t

Epichoroidal stars, 50f

 

Distal (anatomic direction), 3

Epimysium, 182

 

Dorsal (anatomic direction), 3

Epiphora, 162b

 

Dorsal tegmentum, injury, 265

Episclera, 30

 

Dorsonasal artery, 202, 209

connective tissue layer, 30

 

branch, 209

Epithelial cells

 

Drug-induced mydriasis, 260b

adaptation, 5

 

Drugs, impact, 259–260

classification, 5

 

Drusen

 

cytoplasm, iron deposits, 35b

 

confluence, 58f

lateral membranes, connection, 94

 

scattering, 58f

Epithelial iris layers, light micrograph, 46f

Index 279

Epithelial tissue, 5 sheets, 5

Epithelium, 10–12, 23–24 cell turnover, 26 composite drawing, 96f cytoplasm, 45f

layers, 42

apex to apex position, 51 pigment, loss, 58 replacement, 12–13

Epithelium-fiber interface (EFI), 95–96 Equator, cells (mitosis), 127–128 Ethmoid arteries, 202, 205–207 Ethmoid bone, 144

characteristic, 148 impact, 149 orbital plate, 149

Excyclorotation, 184–185 Exocrine glands, 5 Exophthalmos, 158b

External carotid artery, 210–212 branches

flow chart, 213f

ocular adnexa supply, 212f terminal branch, 210–211

External collectors, 50f External hordeolum, 171f

External limiting membrane (ELM), 62f, 71 Extraocular muscles, 139–140

action, 194t

aging changes, 199–200 assessment, 196b blood supply, 211t

denseness, 183 clinical evaluation, 190 enlargement, 197b evidence, 140f

fatigue resistance, 183–184 fibers

layers, organization, 189–190 sizes, range, 183–184

types, divisions, 190 inferior branch, 199 innervation, 189t, 195 insertions, 188f, 194t

macroscopic anatomy, 185–190 muscle length, changes, 199f origin, 194t

structure, 183–184 superior branch, 199

Eyeball, vertical meridian, 156f Eyebrows, 159

components, 159

control, forehead muscles (impact), 160f Eyelids (palpebrae), 139, 159–172

assessment, biomicroscope (usage), 4–5 blood supply, 172

closure, 160f, 178 conditions, 171b

Eastern Asian descent, 160 eversion, 164b

fluid accumulation, 165b glands, 165

histologic features, 165–171 innervation, 171–172 margin, 161

light micrograph, 170f mucocutaneous junction, 173 parts, division, 161

muscles, 165–167 palpebral portion, 161–162 ptosis, 230f

sagittal section, 163f, 166f

Eyelids (palpebrae) (Continued) structures, 161–165

surface anatomy, 160f tarsal plate (tarsus), 164 topography, 160

Eye movements, 184–185 control, 227

direction, 196f result, 184

Eyes, 1–4 accommodation, 53b adduction, 192 anatomic features, 1–2 anterior chamber, 1

anterior surface, team film (spreading), 159 blood supply, 206f

blunt trauma, 40b chambers, 1

ciliary circulation, horizontal section, 208f coats/tunics, 1

duction, movement, 185f early development, 125f

full thickness, photomicrograph, 52f human embryo, light micrograph, 139f layers, 1

neural layer, 61

optical components, image focus, 4

outer connective tissue coat, appearance, 10 posterior chamber, 1

primary position, 198f movements, 192

proptosis, 158f protection, 1

secondary positions, movements, 192–193 sensory nerves, supply, 218

slit-lamp examinations, 118f sympathetic innervation, 268f vascular layer, 1

vitreous chamber, 1

F

Face, bones, 144–148 Facial artery, 210 Facial nerve

cranial nerve VII, 227–231 pathway, 227–231

illustration, 228f temporal/zygomatic branches, 171–172

Facial nuclei (facial nucleus), 227 sagittal section, 225f

Far peripheral retina, ganglion cells, 68f Fascia bulbi (Tenon’s capsule), 175 Fascial expansions, 187

Fat cells, 5

Fenestrated capillaries, network, 55 Fenestrations, presence, 135

Fetal fissure, 124 closure, 134 Fetal lenses, 98f Fetal nucleus, 98f inclusion, 96

Fiber layer of Chievitz, 130–131, 132f–133f Fiber orientation, visual fields

(relationship), 240–249 Fibers, 95

components, 100–101 elastic-like network, 115 epithelium interface, 95–96 formation, 101

inhibitory feedback, 265 interruption, 247f junctions, 101

membranes, interdigitation, 101

280

Index

 

 

 

 

 

 

 

 

Fibroblasts, 5

G

 

branching processes, 40

Gamma-aminobutyric acid (GABA), inhibitory neurotransmitters,

 

diagram, 17f

78–79

 

presence, 119

Gamma proteins, stabilization, 100–101

 

sclera, 52

Ganglion cells, 67–68

 

superficial layer, 42f

amacrine cells, differentiation, 131

 

Fibrovascular tissue, radial projections, 34

axon, 68

 

Fick axes, illustration, 185f

information, 77

 

Fick’s axes, 184

classification, 67

 

eyes, secondary position, 195f

interruption, 135f

 

globe movement, 193f–194f

layer, 62f, 74

 

Filtration apparatus, function, 111

establishment, 131

 

Fissures, 153

neural signal, 68

 

Fixation line, traces, 199f

population, apoptosis (occurrence), 138

 

Fixed, dilated pupil, 266b

synaptic contacts, 74f

 

Flat bipolar cells (FB), processes, 73f

thinning, 132f–133f

 

Flat bipolars, 66–67

types, 68f

 

Flat midget bipolar cell, invaginating midget bipolar cell

Gap junctions

 

­(comparison), 66

appearance, 135

 

Floor, 148–149

formation, 8–9

 

apex, relationship, 149

proteins, 102

 

characteristics, 148–149

Gaze, positions, 185

 

Flow out (Fout), inclusion, 115

Gaze muscles, cardinal positions, 199f

 

Fluid accumulation, 165b

Genetic implications, 141

 

Fluorescein angiography, 205b–207b

Geniculocalcarine pathway, architecture (schematic representation),

 

serial fundus photos, 210f

249f

 

Foramen ovale, 147–148

Geniculocalcarine tract (optic radiations), 237–238

 

Foramen rotundum, 147–148

Germinal zone, 94–95

 

Foramen spinsoum, 147–148

Giant cone bipolar cell, name (derivation), 67

 

Foramina, presence, 149

Giant papillary conjunctivitis (GPC), 175b

 

Forced duction test, 197b

Glands, secretion classification, 5

 

Forehead, lateral aspect (sensory

Glands of Moll, 165

 

fibers), 222

development, 139

 

Forehead, muscles, 159

location, 170

 

control, 160f

presence, 171f

 

sensory fibers, 221

Glandular epithelium, 5

 

Fornices, branch supply, 174

Glaucoma, 116b

 

Fossa, 148

 

drugs, usage, 116

 

Fourth nerve palsy OS, 230f

surgical treatment, 116b

 

Fovea

 

treatment, 116

 

annular zone, 86

carbonic anhydrase inhibitors, usage, 116

 

capillary-free zone, 84

surgical procedures, 116b

 

cells, 69f

Glial cells, proliferation, 130

 

Macaca mulatta, 135f

Glial tissue, 131f

 

Fovea (fovea centralis), 84

band, formation, 138

 

Foveal development, stages, 131–133

Globe

 

Foveal region, light micrograph, 85f

anterior segment, periphery, 41f

 

layers, presence, 85f

anterior surface, tear film coverage, 176

 

Foveal retina, ganglion cells, 68f

coverage, 159

 

Foveola, 84–86

eyelid margin, relationship, 161

 

diameter, 84–85

intraorbital (postluminar) length, 233

 

maturation, 133

lateral side, 186f

 

Free radicals

movement, 193f

 

accumulation, impact, 104

muscles, division, 182

 

by-product, 100

orbital apex, 187f

 

Frontal bone

outside, assessment, 4–5

 

formation, 147

posterior ciliary arteries, entry, 57

 

impact, 148

posterior portion, 220f

 

Frontalis, 159

veins, drainage, 214f

 

Frontal nerve, 186, 221

Glucose (metabolism), aerobic glycolysis (usage), 25

 

location, 188

Glutamate (Glu)

 

Fuchs’ crypts, 43

excitatory neurotransmitter, 78–79

 

presence, 46f

receptors, 80

 

Fuchs’ dystrophy, 24b

release, 79

 

Fuchs endothelial dystrophy, 23f

Glutathione

 

Fundus

 

impact, 104

 

AMD, presence, 58f

reducing agent, 102

 

examination, ophthalmoscope

Glycine, inhibitory neurotransmitters, 78–79

 

(usage), 4

Glycosaminoglycan (GAG) side chains, 16

 

Optomap, 77f

Goblet cells

 

photograph (right eye), 207f

light micrograph, 168f

 

retinal drusen, scattering, 58f

mucus, release, 168

 

Furrows of Schwalbe, 43–46

Goldmann applanation tonometry, performing, 116b

 

 

Index

281

 

 

 

 

 

 

 

Golgi apparatus, 61

Hyaloid vasculature, formation, 128–130

 

 

 

observation, 45f

Hyaluronic acid (HA) (hyaluronan), 119

 

 

 

Golgi tendon organs, 184

Hydrogen ions, buildup, 25

 

 

 

Gonioscopy, 111b

Hydrophobic lipid layer, 6

 

 

 

optical principles, 96f

Hydroxyamphetamine

 

 

 

Graves disease

impact, 259–260

 

 

 

asymmetric signs, 158f

test, 269f

 

 

 

hyperthyroidism, 197b

Hyperopia (farsightedness), 4f

 

 

 

Greater wing, projection, 147–148

correction, 4

 

 

 

Growth factors, presence, 101

Hyperpolarization, magnitude, 79–80

 

 

 

Guttata, 21b

Hyperpolarizing bipolar cells (HBCs), 80

 

 

 

evidence, 23f

Hyperthyroidism (Graves’ disease), 197b

 

 

 

H

Hypophyseal fossa (sella turcica), 147

 

 

 

Hypoxic cornea, oxygen supply (reduction), 25

 

 

 

Hair follicles

I

 

 

 

development, 139

 

 

 

light micrograph, 171f

Immune privilege (establishment), corneal avascularity (impact), 28

 

Haller’s layer, 52–53

Impulse conduction speed, myelinization (impact), 6

 

 

 

Hassall-Henle bodies, 21b

Incongruent right homonymous hemianopia, 247f

 

 

 

increase, 35

Incyclorotation, 184–185

 

 

 

Head

Induction, 127

 

 

 

circulation, 202

occurrence, 127

 

 

 

Head, blunt trauma, 40b

Inferior (anatomic direction), 3

 

 

 

Hemidesmosomes, 8, 11

Inferior extraocular muscles, sheaths, 156

 

 

 

control, 26

Inferior eyelids, 209

 

 

 

impact, 11

aponeurosis, sheaths, 156

 

 

 

Henle layer, 135f

Inferior oblique muscle, 189

 

 

 

Herpes zoster, 221b

action, 192

 

 

 

Heterochromia, 47b

fibers, 225

 

 

 

HIAT, lollipop terminals, 69f

insertion, 189

 

 

 

High intraocular pressure (high IOP), 26b

origin, 189

 

 

 

Histologic features, 5–6

Inferior ophthalmic vein, 214

 

 

 

Holocrine glands, 5

Inferior orbital fissure, 153

 

 

 

meibomian glands, 169–170

Inferior orbital margin, formation, 150

 

 

 

Homonymous field, 244b–245b

Inferior rectus muscle, 188–190

 

 

 

congruent defects, 246b

fibers, 225

 

 

 

incongruent defects, 244b–245b

location, 189

 

 

 

Hordeolum, 171b

Inferior retina, superior field (imaging), 245f

 

 

 

external hordeolum, 171f

Inferior retinal artery, 87

 

 

 

Horizontal cells, 68–69

Information processing, 68–69

 

 

 

communication, 81

occurrence, 218

 

 

 

information transfer, 68–69

Infraorbital groove, 149

 

 

 

whole-mount views, 69f

Infraorbital nerve, 221–222

 

 

 

Horizontal rectus muscles, 192

Infraorbital vein, 215

 

 

 

Horner pupil, iris heterochromia, 267b–270b

formation, 215

 

 

 

Horner’s muscle, 155

Inhibitory message, passage, 81

 

 

 

Horner syndrome, 267b–270b

Inion, 144b

 

 

 

anisocoria, 269f

Inner collagenous zone, 53

 

 

 

cocaine test, 269f

Inner epithelial layer, 51

 

 

 

differential diagnosis, 267b–270b

Inner fiber, 64

 

 

 

hydroxyamphetamine test, 269f

Inner limiting membrane, 74

 

 

 

iris heterochromia, 268f

Inner neuroblastic layer, vitread portion (cell differentiation), 131

 

left eye, dilation lag, 269f

Inner nonpigmented epithelium, growth, 135

 

 

 

miosis, presence, 268f

Inner nuclear layer (INL), 62f, 72–73

 

 

 

presenting anisocoria, 269f

Inner plexiform layer (IPL), 62f, 73–74

 

 

 

ptosis, presence, 268f

axon terminal, 67f

 

 

 

Human cellular physiology, review, 6–9

synaptic contacts, 74f

 

 

 

Human embryo

Inner retinal components, displacement, 131–133

 

 

 

eye, light micrograph, 139f

Inner segment, 64

 

 

 

orbit, 139f

Inner synaptic layer, 73–74

 

 

 

Human LGN, anatomic structure, 242

Innervation, 198

 

 

 

Human retina

blood supply, relationship, 198–199

 

 

 

horizontal cells, whole-mounted views, 69f

Integrins, 7

 

 

 

rods/cones, distribution, 78f

Intercellular junctions, 7–9

 

 

 

Hyalocytes, 119

construction, adhesion molecules (requirement), 35

 

 

 

Hyaloid arterial system, 128–130

protein components, 7

 

 

 

light micrograph, 129f

Intercellular space, acid-rich mucoprotein, 7–8

 

 

 

Hyaloid artery, persistence, 131f

Intermediary tissue of Kuhnt, 138

 

 

 

Hyaloid channel, 118

Intermediate zone, 118

 

 

 

Hyaloideocapsular ligament (of Weigner), 117

Intermuscular septa, 190

 

 

 

Hyaloid system

Internal carotid artery, 202

 

 

 

vessels, atrophy, 130f

branches, flow chart, 213f

 

 

 

vitreous development/regression, 130f

entry, 128–130

 

 

282

Index

 

 

 

 

 

 

 

 

Internal carotid artery (Continued)

Iris (Continued)

 

lateral wall, 227

minor circle

 

location, 215f

arcades, 44f

 

sclerosis, 202b

contribution, 137

 

Internal collector channel (of Sondermann), 95f, 113

mioisis/mydriasis, movement, 41

 

drawing, 100f

pigmented epithelial layers, defects (retro-

 

Internal limiting membrane, 74–75

illumination), 47f

 

fundus view, 75b

posterior surface, radial folds/circular furrows, 49f

 

Interphotoreceptor matrix (IPM), 62–63

pupillary margin, 40

 

carrier proteins, transport, 80

pupillary portion, 44f

 

formation, 75–76

removal, 100f

 

provision, 63

retro-illumination, 47f

 

Interplexiform neurons, 69–70

root, tissue movement, 43

 

cell body, 69–70

sphincter muscle, 40–42

 

long axon, 72

stroma, 40–42

 

processes, 66

surface layer, 40

 

Intracellular communication, network, 83

surfaces, 46f

 

Intracellular pH (decrease), hydrogen ion buildup (impact), 25

synechiae, 43b

 

Intraocular lens (IOL), insertion, 104b

Iris process, presence, 31f

 

Intraocular optic nerve, 235f

Irregular astigmatism, 10b

 

Intraocular pressure (IOP), 97

Isolated agonist model, 190–197

 

changes, impact, 56

Isotropic band (I band), 182

 

circadian fluctuation, 56

J

 

decrease, 99

 

elevation, 26b

Junctional complexes, 8f

 

fluctuations, 115

Juxtacanalicular connective tissue, 110–111

 

impact, 115f

Juxtacanalicular tissue (JCT), 115

 

measurement, 116b

K

 

passive force, 62

 

Intraorbital (postlaminar) length, 233

Keratin fibers, 6

 

Intrinsic muscles, pharmacologic responses, 258–260

Keratin sulphate (KS), 16

 

Invaginating midget bipolar cell, flat midget bipolar cell

Keratoconus, 18b

 

(comparison), 66

photograph, 19f

 

Invagination, synapses, 78

Keratocytes (corneal fibroblasts), characteristics, 16

 

Involuntary muscle tissue, 6

Keratoplasty, 28b

 

Involutional (senile) ectropion, 162f

Krebs cycle, usage, 25

 

Involutional (senile) entropion, 162f

Kuhnt, intermediary tissue, 138

 

Ion channels, 22–23

Kuhnt, tissue (formation), 138

 

Ion cotransporters, 22–23

L

 

Ion flow, mechanisms (schematic), 56f

 

Ionic channels, opening, 182

Lacrimal artery, 204

 

Ionic current, 101–102

branch, 202

 

schematic, 102f

continuation, 204

 

Ion movement, depiction, 25f

location, 188

 

Ion transport, 24

Lacrimal bone, 148

 

Ipsilateral inferior temporal retinal fibers, 241–242

Lacrimal drainage system, anatomy, 178f

 

Ipsilateral (temporal) retina, termination, 244f

Lacrimal gland

 

Iridectomy, 42b

autonomic innervation, 256–258

 

Iris, 40–47, 137

components, 176–177

 

aging changes, 58

development, 140

 

anterior border layer, 40

fluid, secretion, 177

 

absence, 40

lacrimal artery supply, 177

 

anterior layers, 42f

orbital portion, 176

 

anterior segment, light micrograph, 42f

palpebral portion, 176

 

arterial circle, formation, 135

parasympathetic innervation, 255f

 

arteries, branches, 41

portions, division, 176

 

ciliary portion, light micrograph, 46f

sympathetic innervation, 234f

 

coloboma, 128f

Lacrimal lake, 159

 

color, 46–47

Lacrimal nerve, 186, 221

 

cross-section, 46f

Lacrimal sac, 178

 

diaphragm function, 53

fossa, anterior/posterior crest, 154f

 

dilator

 

isolation, 155

 

sympathetic innervation, 254f

pressure, increase, 178–179

 

sympathetic stimulation, 254

theories, difference, 179

 

equilibrium, 256b

Lacrimal secretory system, 176–177

 

functions, 53

Lacrimal system, aging changes, 179

 

heterochromia, 47b

Lacrimation (increase), parasympathetic stimulation

 

congenital Horner syndrome, 268f

(impact), 256

 

Horner pupil location, 267b–270b

Lagophthalmos, 159b

 

histologic features, 40–43

eyelid opposition, inability, 160f

 

layers, 46f

Lamellae

 

light micrograph, 41f

arrangement, 16

 

location, 40

summary diagram, 17f

 

 

Index

283

 

 

 

 

 

 

 

Lamellar synapses, 132f–133f

Lens (Continued)

 

 

 

Lamina cribrosa, 32

vascular supply, absence, 95

 

 

 

impact, 32b

vesicle

 

 

 

scleral perforations, 234

formation, 127–128

 

 

 

Laminae

light micrograph, 129f

 

 

 

crossed retinal projections, termination, 238f

zonule, relationship (diagram), 94f

 

 

 

selective partial involvement, 238f

Lens fibers, 95

 

 

 

uncrossed retinal projections, termination, 238f

arrangement, 99

 

 

 

Lamina fusca (suprachoroid lamina), 52

cells, hexagonal cross-sectional profiles (scanning electron

 

 

 

Lamina papyracea, 149

micrograph), 97f

 

 

 

Laminar optic nerve, 236f

components, 100–101

 

 

 

Laser-assisted in situ keratomileusis (LASIK),

cytoplasm, protein concentration, 95

 

 

 

usage, 29b

formation, 101

 

 

 

Lateral (anatomic direction), 3

process, complexity, 101

 

 

 

Lateral geniculate nucleus (LGN), 237, 242

junctions, 101

 

 

 

anatomic structure, 242

production, continuation, 95

 

 

 

blood supply, 240

UVR absorption, 102

 

 

 

coronal section, 238f

Lesser wings, projection, 147–148

 

 

 

layered structure, 237

Levator

 

 

 

relay station, 237

action, 163

 

 

 

retinotopic map representation, 244f

anteroposterior direction, change, 162

 

 

 

Lateral ligaments, upper borders, 165

tendinous expansion, 163

 

 

 

Lateral orbital margin, 150

Levator aponeurosis, 163

 

 

 

Lateral orbital tubercle, 165

Ligand-gated stimulants, 6–7

 

 

 

Lateral orbital wall, bones, 153f

Light adaptation, 82–83

 

 

 

Lateral palpebral arteries, 211f

Light/dark cycle, 83

 

 

 

Lateral palpebral ligament, 165

Light energy transformation, 61

 

 

 

orbital septum, relationship, 155

Light-near dissociation, 265

 

 

 

Lateral rectus muscle, 187–188, 190

Light path, cellular organelles, 99

 

 

 

contraction, abduction, 192f

Light rays, neural signal configuration, 1

 

 

 

superior border, 188

Limbal area, light micrograph, 34f

 

 

 

Lateral wall, 149–150

Limbal blood vessels, 34

 

 

 

characteristics, 149

Limbal conjunctiva, formation, 31f

 

 

 

L-cone cells, opsin (sensitivity), 79

Limbal histologic features, 33

 

 

 

Leaky epithelium, 7

Limbal stem cells

 

 

 

Left eye

deficiency, 34b

 

 

 

Brown’s syndrome, 198f

niche, 34

 

 

 

dilation lag, 269f

Limbal stroma, location/composition, 110f

 

 

 

fundus, 88f

Limbus, 32–35

 

 

 

OS, third nerve palsy, 230f

anterior boundary, components, 32

 

 

 

proptosis, 158f

area, light micrograph, 34f

 

 

 

Left internal carotid artery, CT scan, 248f

blood vessels, lymphatics, 34

 

 

 

Left medial canthus, structures, 160f

corneoscleral junction location, 32

 

 

 

Left orbital floor, blow-out fracture

drawing, 110f

 

 

 

(coronal CT), 152f

histologic features, 33

 

 

 

Lens, 127–134

illustration, 31f

 

 

 

biconvexity, 93

innervation, 220f

 

 

 

capsule, 93–94, 100

stem cell deficiency, 34b

 

 

 

light micrograph, 97f

transition, 33

 

 

 

transparency, 93–94

transitional zone, 32–33

 

 

 

cells, bands, 98f

Line of fixation, traces, 199f

 

 

 

cortex, thickness, 98–99

Lipids

 

 

 

curvature, 98–99

bilayer, ion movement (facilitation), 6–7

 

 

 

development, protein manufacture, 100–101

double layer, 6

 

 

 

dimensions, 93

Lockwood (suspensory ligament), 156

 

 

 

divisions, 96

Lollipop terminals, 69f

 

 

 

epithelium, 94–95

Long ciliary arteries, anastomosing, 135

 

 

 

fiber interface, 95–96

Long ciliary nerve, 220f

 

 

 

protection, ascorbic acid (impact), 102

formation, 220

 

 

 

fiber membranes, cholesterol content, 101

Long-standing immobility, 197b

 

 

 

glucose, collection, 101

Loose connective tissue, 5

 

 

 

ionic current, schematic, 102f

Lower eyelids

 

 

 

metabolism, 101

aponeurosis (capsulopalpebral

 

 

 

optic section, 99b

fascia), 163

 

 

 

paradox, 103b

canaliculi, 178

 

 

 

physiology, 99–102

light micrograph, 171f

 

 

 

placode, 127

meeting, 159

 

 

 

formation, 129f

rectractor, 163

 

 

 

thickening, 129f

sensory innervation, 221f

 

 

 

posterior vascular tunic, formation, 128–130

Lumen, endothelial cell lining, 110

 

 

 

refractive power, 93

Lymphatic drainage, 216

 

 

 

slit-lamp appearance, 99b

Lymphatics, 34

 

 

 

sutures, 96–97

Lymphocyte, presence, 14f

 

 

284

Index

 

 

 

 

 

 

 

 

M

 

Meshwork trabeculae, components, 109–110

 

Macaca mulatta, fovea, 135f

Mesoderm, impact, 123

 

Macaque monkey, lateral geniculate nucleus (coronal section), 238f

Metabolic retina, nutrients (loss), 57b

 

Macromolecules, concentration, 55

Metabolic transport mechanisms, site, 94

 

Macrophages, 5

Metamorphopsia, 85b

 

alteration, 40

Meyer loops, passage, 244f

 

Macula lutea, 83–84

Microglia, phagocytic properties, 6

 

terminology, 84b

Microglial cells, 70

 

Macular adherens (MA), 7

Microphthalmic eye, result, 127

 

Macular areas

Microplicae, 168

 

fibers, termination, 244

Microtubules, 6, 101

 

terminology, 84b

Microvilli, 168

 

Macular degeneration, age (relationship), 57b

Midbrain

 

Macular occludens (MO), 7

dorsal tegmentum, injury, 265

 

intercellular junctions, 45f

lesion, impact, 265

 

Macular region, capillary bed, 85f

oculomotor nucleus, 224

 

Macular sparing, 248–249

Middle retina, ganglion cells, 68f

 

occurrence, 248–249

Midget bipolar cell, 66

 

Madarosis, 161b

Midsagittal (anatomic plane), 3

 

Magnetic resonance imaging (MRI), usage, 247

Miosis, 41–42

 

Main lacrimal gland, contribution, 177

presence, 268f

 

Marfan syndrome, 141

Mitochondria, 61

 

Mast cells, 5

Mitosis, occurrence, 26

 

Mastoid process, 144

absence, 27

 

Maxillary artery, 211–212

Mittendorf’s dot, 130b

 

Maxillary bone

Modified apocrine glands, location, 170

 

frontal process, 152

Modified sweat glands, 165

 

orbital plate, 148–149

Moll glands, presence, 171f

 

Maxillary nerve formation, 222

Motor nerves, efferent pathway, 224–231

 

Medial (anatomic direction), 3

Müller (orbital muscle), 157

 

Medial canthal area, structures, 218

Müller (tarsal muscle), development, 139

 

Medial canthus, 159

Müller cells, 70

 

Medial ligaments, upper borders, 165

fibers, appearance, 131

 

Medial orbital wall, bones, 152f

hypertrophy, 89

 

Medial palpebral arteries, 202, 209

pervasiveness, 70

 

branches, 211f

structure, 72f

 

Medial rectus muscle, 187, 190

Müller muscle

 

contraction, adduction, 192f

contractions, 163–164

 

fibers, 225

sympathetic innervation, 234f

 

Medial wall, 149

Müller’s annular muscle, 48

 

characteristics, 149

Munson’s sign, 18b

 

formation, ethmoid bone (impact), 149

photograph, 19f

 

Medulla oblongata, 227

Muscle contraction

 

Meibomian glands

association, 198

 

anatomy, 166f

initiation, 259

 

development, 139

sliding ratchet model, 182–183

 

holocrine glands, 169–170

illustration, 184f

 

infrared digital photography, 166f

Muscle length, changes, 199f

 

light micrograph, 169f

Muscle movement, line (relationship), 195f

 

loss, grading scales, 166f

Muscle of Müller, 163

 

occupation, 169

contraction, 163–164

 

pores, location, 161

Muscle spindles, 184

 

secretion, 170

Muscle tissue, 6

 

tarsal glands, 165

classification, 6

 

Meibomianitis, 177b

Muscular arteries, 202, 207

 

Melanin

 

variation, 207

 

granules

Myasthenia gravis, 183b

 

density, 46–47

Mydriasis, 41

 

presence, 168

Myelin, 6

 

production, 133b

Myelinated nerve fibers, 6

 

Melanocytes

Myelinization, impact, 6

 

branching processes, 40

Myofibrils

 

choroidal stroma, 52

anisotropic band (A band), 182

 

pigment, derivation, 133b

isotropic band (I band), 182

 

Melanosomes, 61

Myofibrils, types, 182

 

Membrane-bound organelles, degradation, 101

Myofilaments, proliferation, 137

 

Membrane-spanning proteins, 7

Myopia

 

Meningeal sheath, 202–203

refractive error, reduction, 29b

 

Mesenchymal cells, alignment, 137

Myopia (nearsightedness), 4f

 

Mesenchyme, 124

correction, 4

 

covering layers, 125f

Myopic refractive error, reduction, 29b

 

proliferation/migration, 127, 135

Myosin

 

Meshwork, anatomic divisions (separation), 109

actin junction, breakage, 183

Index 285

Myosin (Continued)

ATP attachment, 182 myofibrils, 183f

Myosin fibers, 6

N

Na/K/ATPase pumps, location, 6–7 Nasal bones, impact, 148

Nasal direction-adduction, 192 Nasal fibers, travel, 240

Nasal step, 246b

automated visual field, 247f Nasociliary nerve, 222f

formation, 221

Nasolacrimal drainage system, 140, 178 Nasolacrimal duct, 178

Nasolacrimal system, 140

Near-point reaction (accommodation-convergence reaction), 260–261

Near pupillary response, 263f Neck

circulation, 202

internal carotid artery, contact, 202 Nerve fiber layer (NFL), 62f, 74 Nerve fiber orientation, 241f

Nerve tissue, 6 cell types, 6

Nervous system, 218 Neural cells

death, 249–250 number/distribution, 78

Neural crest cells differentiation, 135 separation, 124f

Neural ectoderm, invagination, 51 Neural fold, growth, 124f

Neural groove, invagination, 124f Neural retina, 130–134

Neural signals, 76–77 Neural tube

formation, 124f

inner surface, indentations, 123–124 Neuroblastic layers, formation/completion, 130–131 Neuroglia, 6

Neuroglial cells, 70

number, neuron number (comparison), 6 Neuronal cell bodies/processes, 70 Neurons, 6

Neurotransmitters, 78–79, 258–259 action, drug replication, 259

Neurotrophic keratitis, 28b

Nonpigmented cells, basal/basolateral aspects, 51 Nonpigmented ciliary epithelium (NPE), 51, 55

basolateral membrane, ions (exit), 55–56

Nonpigmented epithelium, internal limiting membrane, 111 Nonproliferative diabetic retinopathy, OD (fundus photo), 75f Norepinephrine

recycling, 259 release, 260f

Nuclear cataracts, 103b–104b presence, 105f

Nuclear sclerotic cataract (NSC), 120

O

Oblique muscles, 192–193 complexity, 198

Occipital bone, 144 impact, 144

Occipital lobe striate cortex, 239f

visual area/striate cortex, 239f Occipital lobe, visual pathway, 239f Occludin, 7

Occluding junction, 7 Ocular adnexa

lymphatic drainage, 216f structures, 159

supply, external carotid artery branches, 212f Ocular adnexa, development, 138–140 Ocular albinism, 133b

Ocular circulation aging, effect, 216 physiology, 209–210

Ocular coherence tomography (OCT) scan, right macular area, 86f Ocular development/mutation, RAX (impact), 141

Ocular motility testing, 196b Ocular movement terminology, 186t Ocular structures

development, 123–138 embryologic derivation, 123b genetic implications, 141 parasympathetic pathway, 255–256 sympathetic system supply, 253

Ocular structures, sympathetic pathway, 233–236 Oculocardiac reflex, 224b

Oculomotor damage, 229b Oculomotor foramen, 186 Oculomotor nerve

cranial nerve III, 224–225 exit, 225

nuclei, lateral/dorsal views, 225f pathway, 225

regeneration, aberration, 229b sagittal section, 225f

Oculomotor nucleus, 224–225 midbrain location, 224

OFF bipolars, 80

OFF cells, designations, 80 Oligodendrocytes, 6

ON bipolars, 80

ON cells, designations, 80

Opaque cornea, collagen fibrils (orientation), 17f Ophthalmic agonist agents, 259–260 Ophthalmic antagonist agents, 260

Ophthalmic artery, 188, 202–210 branches, 202

orbit, view, 203f origin, order, 204t terminal branch, 209

Ophthalmic Graves disease, asymmetric signs, 158f Ophthalmic instrumentation, 4–5

Ophthalmic nerve formation, 221 orbit, 219f

Ophthalmoscope, usage, 4 Opsin, formation, 79 Optic chiasm, 236–237

blood supply, 240 fibers

exit, 241–242 orientation, 242f

sagittal section, 237f

third ventricle, floor, 236–237

vessels of circle of Willis, relationship, 236f Optic cup, 127–134

cell layers, 127

inferior surface, views, 126f

inner layer, basement membrane, 130–131 internal carotid artery entry, 128–130 layers, apposition, 130

lip, elongation, 137 longitudinal section, 126f

outer layer, pigment (evidence), 140f surface, glial cells, 130

Optic disc, 86–87, 240–241 assessment, 87b

286 Index

Optic disc (Continued) glial tissue, 131f margins, flatness, 87

peripapillary adhesion, 117 retinal elements, absence, 86

surface, nerve fiber orientation, 241f Optic fissure, 124

closure, 126f

Optic nerve, 138, 233–236, 241 capillaries, 239–240 choroid, connection, 51–52 cupping, 32b

damage, 154b formation, 126f head, 86

elevation, 88f

surfaces, three-dimensional mapping, 5 inferior branch, 225

intraocular section, 233 longitudinal section, 205f meningeal sheaths, 233–234 passage, 32

Optic neuritis, 265b Optic pits, 123–124 Optic radiations

nerve fiber bundles, 249f striate cortex projection, 249f

Optic radiations (geniculocalcarine tract), 237–238, 243 anterior radiations, 240

divisions, 240

fibers, middle group, 240

posterior cerebral artery, branches, 240 result, 247f

Optic stalk buckling, 124

fetal fissure, closure, 134 longitudinal view, 126f transverse sections, 126f

Optic strut, 153

Optic tract, 237, 241–242 Optic vesicle

buckling, 124 evagination, 124

Optomap, fundus (display), 77f Ora, bays/dentate processes, 49f Ora serrata

choroid, connection, 51–52 light micrograph, 52f

retina, peripheral termination, 86

RPE basement membrane, continuity, 53 Orbicularis ciliaris (pars plana), 47 Orbicularis muscle, motor control, 171–172 Orbicularis oculi, 159

action, 162 muscle, 161–162 orbital portion, 162

palpebral portion, 161–162 Orbit, 139, 148–158

aging changes, 158 blow-out fracture, 149b bones, anterior view, 150f composition, 148 connective tissue, 154–158

arrangement, 154 drainage, 214f fascial system

horizontal section, 157f vertical section, 156f

horizontal section, 154f lateral view, 214f

lateral wall, formation, 147 nerves, 155f

ophthalmic artery, branches, 203f

Orbit (Continued) section, 139f shape, 148

sinuses, relationship, 154 veins, 212–216

vessels, 155f

Orbit, separation, 149–150 Orbital adnexa, aging changes, 179 Orbital apex, 187f

globe, removal, 226f Orbital area, viewpoint, 164f Orbital cellulitis, 154b

Orbital connective tissue structures, 190 Orbital cranial nerves, 219t

Orbital fat, 157–158 derivation, 139

Orbital floor, bones, 151f Orbital foramina/fissures, 153 Orbital margins, 150–152

spiral shape, 154f

Orbital muscle of Müller, 157 Orbital optic nerve, 235f

Orbital periosteum (periorbita), 155 Orbital plate, 148–149

Orbital roof, bones, 151f

Orbital sensory innervation, 218–224 Orbital septal system, 157

Orbital septum, 155–156

lateral palpebral ligament, relationship, 155 medial margin, 155

removal, 164f Orbital walls, 148–150

angular relationship, 149f damage, 152f

sinus cavities, location, 155f Outer collagenous zone, 53 Outer fiber, 64

Outer neuroblastic layer, components, 132f–133f Outer nuclear layer (ONL), 71

Outer plexiform layer (OPL), 62f dendritic tree, 69f

synapses

linear arrangement, 132f–133f occurrence, 78

Outer retina (nutrient supply), vascular choroid (usage), 57 Outer synaptic layer, 72

Outflow channels, anatomy, 97f Outflow pathway, resistance, 115 Overnight corneal swelling, 25b Oxidative stress

induction, ROS (impact), 27 UVR, relationship, 102

Oxygen depletion, supply, 28b Oxygen supply

closed eye conditions, 24 reduction, 25

P

P2 ganglion cell, termination, 67 Paired antagonist model, 197–198 Paired obliques, primary actions, 198 Palatine bones, 148

Palisades of Vogt, 34–35

fibrovascular tissue, radial projections, 34 limbal stem cell niche, 34

niche, 34

Palpebrae (eyelids), 139, 159–172 Palpebral blood supply, 173f Palpebral conjunctiva, submucosa, 169 Palpebral fissure, 159

Palpebral ligaments, 165 Palpebral muscles, 166f Papilledema, 87b, 214b

Index 287

Parafoveal areas, 86 Paranasal sinuses, 153–154

location, 155t Parasympathetic innervation, 99b

flow chart, 257f–258f impact, 235f

Parasympathetic nucleus, inhibitory feedback, 265 Parasympathetic stimulation

lacrimation, increase, 256 pupillary constriction, 256 Parasympathetic system, 253

activation, 262

Pars plana (orbicularis ciliaris), 47

ciliary epithelial layers, light micrograph, 52f columnar cells, 51

extension, 47

Pars plicata (corona ciliaris), 47 cuboidal cells, 51

PAX2 (gene), mutations, 141 Perichoroidal space, 52

Pericytes (Rouget cells), ability, 53 Perifoveal areas, 86

Perimysium, 182

Periorbita (orbital periosteum), 155 Peripapillary choriocapillaris, 204 Peripapillary chorioretinal atrophy, 89 Peripheral anterior synechia (PAS), 43b Peripheral crypts, 43

Peripheral retina, 86

Peripheral retinal degeneration, 86b Peripheral retinal traction, 119b Peripheral vision, 83b

Persistent pupillary membrane, 137b Petrous portion (temporal bone), 144 Photokeratitis (UVR overexposure), 27b Photon, light (changes), 79

Photopic vision, 76 Photoreceptor cells, 62–66, 71

absence, 86 illustration, 64f neural signal, 68

Photoreceptors activation, 80 dark current, 79f depolarization, 80

glutamate, release, 78–79 hyperpolarization, 80

light stimulation, absence, 79 location, 84 migration/maturation, 131–133 outer segments, growth, 132f–133f

Photorefractive keratoplasty (PRK) removal, 15

usage, 29b Phototransduction, 79–80

photon, change, 79

Physiologic blind spot, scotoma (central visual field plots), 245f Physostigmine, indirect-acting cholinergic agonist, 261f

Pig embryo, light micrograph, 140f Pigmentary dispersion syndrome, 47b Pigmented iris epithelium, transition, 51f

Pigment epithelium derived factor (PEDF), 75–76 Pigment mottling, 58f

Pilocarpine, direct-acting cholinergic agonist, 260 impact, 261f

Pingueculae, 175b connective tissue, 175b photograph, 175f

Pituitary adenoma, CT scan, 248f Plasmalemma, 64–65 Pleomorphism, 20

inclusion, 89

Plexiform layers, appearance, 131

Point-to-point localization (retinotopic map), 242 Poles, 93

Polymegathism, 20 Pons, groove, 227 Positions of gaze, 185

extraocular muscles, innervation, 195 Posterior (anatomic direction), 3 Posterior cerebral artery, branches, 240 Posterior chamber, 111

regions, 97f

Posterior ciliary arteries, 204–207 globe entry, 57

Posterior epithelial cells, elongation, 127–128, 129f Posterior epithelium, 42–43

layers, 45f

lens fibers, relationship, 96 Posterior iris, 41f

epithelial layers, position, 43 surface, 43–46

pigment granules, shedding, 47b Posterior lens capsule, thickness, 94f Posterior lens surface, attachment, 93 Posterior sclera, 33f

globe, posterior portion, 220f

Posterior scleral foramen, optic nerve passage, 32 Posterior subcapsular cataract (PSC), 103b–104b, 106

photograph, 105f

Posterior synechia, pupillary margin involvement, 43b Posterior vascular tunic, formation, 128–130 Posterior vitreal detachment, 119b

Postganglionic fibers ganglion exit, 253 skull entry, 267b–270b

Postlaminar optic nerve, 236f Potassium channels (K+ channels), 6–7

Potassium ions (K+ ions), circulation, 55–56 Precorneal film (retention), microvilli

(involvement), 14f

Preganglionic fibers, dorsal column exit, 267b–270b Preganglionic neuron, location, 255

Prelaminar optic nerve, 236f Prematurity, retinopathy, 134b Presbyopia, 99b, 103

accommodation loss, 55b Presenting anisocoria, 269f Preseptal cellulitis, 155b

Presynaptic membrane, action potential (impact), 6 Primary gaze, 230f

Primary position, 196 movements, 192

Primary visual cortex (striate cortex), 238–239 location, 238

organization, 238 Procerus, 159 Proptosis, 158f Proteoglycans (PG), 16

Proximal (anatomic direction), 3 Pseudoesotropia, origin, 161f Pterygia, 175b

connective tissue, 175b Pterygium

photograph, 176f Pterygium, overgrowth, 175b Pterygoid process, 147–148 Pterygoid venous plexus, 214

Pterygopalatine fossae, 147–148 maxillary nerve formation, passage, 222

Pterygopalatine ganglion, 222 Ptosis, 164b

presence, 268f unilateral ptosis, 164f

Puncta, 178

Pupillary constriction, 256

288

Index

 

 

 

 

 

 

 

 

Pupillary light pathway, 262–270

Retina (Continued)

 

illustration, 264f

absence, 128f

 

understanding, 262

capillary blood flow, 83

 

Pupillary light response, 262b

vertical connections, 81

 

Pupillary margin, 40

vessels, 134

 

involvement, 43b

capillary-free zone, relationship, 87–88

 

Pupillary membrane, 137

visual pathway, 239f

 

persistence, 137b

Retinal blood supply, 87–88

 

R

 

Retinal cells, 71f

 

 

Retinal degenerations, 76b

 

Radial folds, iris, 49f

Retinal detachment, 63b

 

Radial keratotomy (RK), usage, 29b

Retinal drusen, scattering, 58f

 

Radio-labeled substances, turnover (slowness), 100

Retinal function, 75–83

 

RAX (gene), impact, 141

Retinal ganglion cells, axons (patterns), 240

 

Reactive oxygen species (ROS), impact, 27

Retinal hemorrhages, 74b

 

Receptive fields, 82

Retinal histologic features, 61–70

 

center-surround configuration, 82

Retinal layers, 70–75

 

Rectus muscles

Retinal metabolism, 83

 

insertions, 187

Retinal nerve head surfaces, three-dimensional mapping, 5

 

origin, 185–186

Retinal neurons, ON/OFF cells, 80

 

annulus of Zinn, 187f

Retinal pigment epithelium (RPE), 51, 61–62, 71, 130

 

display, 226f

basement membrane, 53

 

tendon, insertion measurements, 187t

continuity, 53

 

Recurrent corneal erosion, 13b

detachment/atrophy, 57b

 

Red eye, 209b

filaments, merging, 53

 

Referred pain, 222b

ion transport, model (proposal), 75

 

Refractive conditions, 4

illustration, 76f

 

examples, 4f

layer, 62f

 

Regular astigmatism, occurrence, 10b

lysosomal activity, decrease, 59

 

Relative afferent pupillary defect (RAPD)

melanin-related agent, production, 133b

 

application, 262

neuroretinal interface, 62–64

 

left eye (RAPD OS), 265f

physiology, 75–76

 

presence (determination), swinging-flashlight test

rods/cells, outer segments (3D relationship), 63f

 

 

(usage), 262

transport systems, lipid accumulation (implications), 58f

 

right eye (RAPD OD), 265f

Retinal pigment epithelium (RPE) cells

 

Retina, 240

apical portion, 61

 

accommodation, 53b

basement membrane, 55f

 

aging changes, 88–89

extracellular space, 62–63

 

blood supply, 87–88

melanosomes, 61

 

cells, 71f

phagocytosis, 75–76

 

circuitry, knowledge, 78–79

Retinal processing, 82

 

coloboma, 128f

Retinal receptive fields, arrangement, 82

 

cone bipolar cells, camera lucida drawings, 67f

Retinal synapses, 71f

 

degenerations, 76b

Retinal tissue

 

detachment, 63b

capillary blood flow, 83

 

development, 132f–133f

venous branches, location, 214

 

flow chart, 134f

Retinal vascular tree, retina nerve fiber pattern (relationship), 241f

 

function, 75–83

Retinal venous branch occlusion, 204b

 

ganglion cells, axons

Retinal vessels, 134

 

growth, 126f

autonomic innervation, absence, 209–210

 

pattern, 240

capillary-free zone, relationship, 87–88

 

hemorrhages, 74b

pacemaker mechanisms, 209–210

 

histologic architecture, 84f

Retinitis pigmentosa, 76b

 

image, orientation, 234f

Retinopathy of prematurity (ROP), 134b

 

layers, 62f, 70–75

Retinotopic map (point-to-point localization), 242

 

light energy transformation, 61

Retrobulbar optic neuritis, 186b

 

light micrograph, full-thickness view, 72f

Retrolental tract, 118

 

light microscopy, imagery, 61

Ribbon synapses, 78

 

metabolism, 83

Ribonucleic acid (RNA) granules, protein manufacture, 6

 

nerve fiber pattern, 241f

Right eye

 

neural tissue, 1

fundus photograph, 207f

 

nutrients, loss, 57b

normal fundus, 75f

 

peripheral termination, 86

papilledema, 88f

 

photoreceptor layer, 62f

proptosis, 158f

 

processing, 82

Right eyelid, surface anatomy, 160f

 

receptive fields, arrangement, 82

Right fundus

 

regions, 83–87

photo, Best’s disease, 77f

 

schematic, 84f

photo, Stargardt’s macular dystrophy, 77f

 

rods/cones, distribution, 78f

Right lateral geniculate nucleus, laminae, 238f

 

stages, 132f–133f

Right macular area, ocular coherence tomography (OCT) scan, 86f

 

synapses, 71f

Right superior oblique dysfunction, 229f

 

ten-layered arrangement, 70

Rods, 64–65

 

tissue

bipolar cell, 66

 

 

Index

289

 

 

 

 

 

 

 

Rods (Continued)

Septa

 

 

 

cells

location, 190

 

 

 

body, 64

presence/orientation, 190

 

 

 

outer segments, relationship (3D drawing), 63f

Serial fundus photos, 210f

 

 

 

cilium, 64

Short ciliary nerves

 

 

 

composition, 64

damage, 266

 

 

 

density, increase, 78

location, 256

 

 

 

distribution, 78f

Sinus cavities, location, 155f

 

 

 

inner fiber, 64

Sixth nerve palsy OS, 231f

 

 

 

inner segment, 64

Skin, 165

 

 

 

junction, 65f

sensory fibers, 218, 221

 

 

 

width, 65

Skull

 

 

 

light detection, 76

anterior view, 146f

 

 

 

morphology, 64–66

base, disarticulated view, 147f

 

 

 

outer fiber, 64

bones, unification, 144

 

 

 

outer segment, 64

division, 144

 

 

 

junction, 65f

floor, 146f

 

 

 

width, 65

lateral view, 145f

 

 

 

spherule, 66f

ophthalmic/maxillary divisions, entry, 223

 

 

 

synapses, 66f

posterior aspect (formation), occipital bone (impact), 144

 

 

 

Roof, 148

posterior view, 145f

 

 

 

characteristic, 148

Slings, connective tissue system, 157

 

 

 

Rouget cells (pericytes), ability, 53

Smooth endoplasmic reticulum, 61

 

 

 

Rough endoplasmic reticulum, 61

Smooth ER, impact, 6

 

 

 

Rough ER, impact, 6

Smooth muscle tissue, 6

 

 

 

S

Sodium channels (Na+ channels), 6–7

 

 

 

Sorbitol concentration, increase, 104–105

 

 

 

Sagittal (anatomic plane), 3

Space filler, 5

 

 

 

Sarcomere

Spaces of Fontana, 109

 

 

 

extension, 182

Sphenoid bone, 144, 147

 

 

 

thick/thin filaments, arrangement, 183f

greater wing, 149–150

 

 

 

Sarcoplasmic reticulum, calcium ion release, 182

projection, 147–148

 

 

 

Sattler’s layer, 52–53

lesser wings, projection, 147–148

 

 

 

Schlemm canal, 110–111

Spheroid bone, coronal section, 215f

 

 

 

inclusion, 41f

Sphincter muscle, 40–42

 

 

 

lumen, presence, 31f

location, 41–42

 

 

 

region, 220f

parasympathetic innervation, 255f

 

 

 

Schlemm’s canal, 50f, 109

Spiral of Tillaux, 187

 

 

 

cross-sectional diameter, 116b

rectus muscles, impact, 187f

 

 

 

derivation, 138

Spontaneous venous pulsation, 214b

 

 

 

drawing, 100f

Squamous corneal epithelium, 32–33

 

 

 

inner wall, 110–111

Squamous portion (temporal bone), 144

 

 

 

endothelium, 115

Squamous surface cells, light micrograph, 15f

 

 

 

Schwalbe’s line, 18, 97f

Stargardt’s macular dystrophy, right fundus (photo), 77f

 

 

 

Schwalbe’s ring, 18

Stem cells, niche location, 34

 

 

 

Schwann cells

Steroid-induced cataract, 106

 

 

 

absence, 6

Strabismus, 197b

 

 

 

covering, loss, 27

surgery, 197b

 

 

 

sheath, loss, 14f

Stratum opticum, 74

 

 

 

Sclera, 29–32, 135

Striate cortex (primary visual cortex), 238–239, 243–249

 

 

 

blood supply, 32

maps, 247

 

 

 

bulbar conjunctiva, coverage, 172

projection, 249f

 

 

 

collagen bands, 52

visual information, combination, 239

 

 

 

detachment, 50f

Striated muscle

 

 

 

fibroblasts, 52

connective tissue

 

 

 

formation, 29–30

network, 183f

 

 

 

histologic features, 30

sheath, relationship, 182

 

 

 

innervation, 32

light/dark bands, 182

 

 

 

Scleral nerve loops of Axenfeld, 220b

microscopic anatomy, 182–184

 

 

 

Scleral spur, 50f, 109

photomicrograph, 183f

 

 

 

collagen fibers, presence, 31f

tissue, 6

 

 

 

trabecular sheets, endothelial covering

Stroma, 15–18, 24, 26, 169

 

 

 

(loss), 110

components, arrangement, 16–18

 

 

 

Sclerosis, internal carotid artery, 202b

corneal injury, extension, 26

 

 

 

Scotopic vision, 76

epithelial layer, 42–43

 

 

 

Sebaceous glands of Zeis, sebum (secretion), 165

extracellular matrix, anchoring laminin-containing

 

 

 

Secondary fibers, Y-suture (meeting), 127–128

plaques, 12

 

 

 

Secondary positions, 195f

extracellular water content, control, 22–23

 

 

 

movements, 192–193

sphincter muscle, location, 41–42

 

 

 

Secondary vitreous, development, 138

water, imbibing, 24

 

 

 

Second-order neuron, 66

Styloid process, 144

 

 

 

Sella turcica (hypophyseal fossa), 147

Stylomastoid foramen, 144

 

 

 

Sensory innervation, 221f

Substantia propria, 15–18, 169

 

 

290 Index

Superficial conjunctival cells, surface, 168 Superficial temporal artery, 210–211

terminal branch, 210–211 Superior (anatomic direction), 3 Superior colliculus, 239 Superior eyelids, 209

Superior nasal fibers, superior chiasm entry, 241 Superior oblique muscle, 189

action, 192 length/width, 189 origin, 189

trochlea, impact, 189 Superior ophthalmic vein, 212

angular/supraorbital veins, connection, 212 Superior orbital fissure, 153, 227

edges, 155

medial posterior edge, 153 nerves/vessels, entry, 155f roof separation, 149–150

Superior orbital margin ridge (formation), frontal bone (impact), 148

Superior palpebral levator muscle, 162–163 Superior palpebral sulcus, elimination, 160 Superior rectus muscle, 188

contraction, Fick’s axes (globe movement), 193f innervation, 188

insertion, 188 Superior retinal artery, 87

Superior retinal quadrants, fibers (termination), 242 Suprachoroidal space, 52

Suprachoroidea (suprachoroid lamina), 54f Suprachoroid lamina

lamina fusca, 52 suprachoroidea, 54f

Supraciliaris (supraciliary lamina), 48 sclera, detachment, 50f

Supraorbital artery, 202, 207 origin, 207

Supratrochlear artery, 202, 209 Supratrochlear notch, 150 Supraversion, 185

Surface cells age/degeneration, 11 polygonal shape, 14f

Surface ectoderm, 123 covering layers, 125f

lens vesicle, separation, 127 Suspensory ligament (of Lockwood), 156

connective tissue, 156 Swinging-flashlight test, 262b–265b

response, 265f usage, 262

Sympathetic fibers hypothalamus control, 253 travel, 253

Sympathetic innervation, 268f flow chart, 257f–258f

Sympathetic nerves fibers, presence, 27 plexus, 202

Sympathetic pathway damage, 267b–270b disruption, 266–270 origination, 253

Sympathetic stimulation, impact, 236 Sympathetic system, 253

Synapses, 6

linear arrangement, 132f–133f Synaptic complexes, appearance, 131 Synaptic contacts

arrangements, 73f occurrence, 72

Synaptic densities, 72

Synaptic vesicles, neurotransmitter release, 78 Synkinesis, 260–261

T

Tarsal conjunctiva, 172

Tarsal glands (meibomian glands), 165 Tarsal muscle of Müller, 163–164

development, 139

Tarsal plate, 160, 164–165, 167 Tear drainage, 178–179

Tear film, 21, 176–179 assessment, 177b coverage, 176 distribution, 177–178

goblet cell storage/secretion, 168 schematic representation, 176f spreading, 159

Tear film breakup time (TBUT), 177b Tears

overflow, 162b pooling, 159

Teenagers, right eye (normal fundus), 75f Temporal arteritis, 211b

Temporal bones, 144 composition, 144 petrous portion, 144 squamous portion, 144

Temporal crescent, 244b–245b

Temporal field (physiologic blind spot), scotoma (central visual field plots), 245f

Temporal fossae, 154b Temporal retina, nasal field, 245f Tendinous ring, 185

Tenon capsule, 110f formation, 31f

Tenon’s capsule, 156, 175–176 episclera, connection, 30 fascia bulbi, 175

formation, 176 location, 33 piercing, 156

Terminal bar, 7

zonula occludens/adherens, 61–62 Tertiary vitreous, stretching, 130f Thick myofibrils, 182

Thick-walled blood vessels, 41 Thin myofibrils, 182

Third nerve palsy, left eye OS, 230f Three-layered endothelium, separation, 136f Tissue of Kuhnt, formation, 138 Tonofilaments, 7–8

Torsions, 184–185 movement, questions, 185

Trabeculae, prominence, 46f Trabecular meshwork, 50f, 109–110

configuration (change), ciliary muscle contraction (impact), 53b

inclusion, 41f separation, 109 visibility, 138

Trabecular sheets, pigment/debris deposits, 116b Transepithelial ionic transport, fluid production, 55 Transient fiber layer of Chievitz, 130–131, 132f–133f Transporting epithelia, polarization, 6–7

trans retinol, uptake, 80 Transverse (anatomic plane), 3

Transverse tubules (T tubules), ion spread, 182 Tricarboxylic acid (TCA) cycle, usage, 25 Trichiasis, 161b

Trigeminal ganglion, fibers (exit), 223 Trigeminal nerve

activation, irritation, 256 divisions, 222f

Index 291

Trigeminal nerve (Continued) formation, 223–224 mandibular division, 223 maxillary division, 221–222 ophthalmic division, 218–221 sagittal section, 225f

Trochlea attachment, 148 origin, 189

Trochlear damage, 229b–230b Trochlear nerve

cranial nerve IV, 225–227 entry, 227

pathway, 226–227 sagittal section, 225f

Trochlear nucleus, 225–226 Troponin-tropomyosin complex, calcium

(binding), 182 Tunics (coats), 1 Two-layered epithelium

basal lamina basis, 136f separation, 136f

Tyndall phenomenon, 56b–57b

U

Ultrafiltration, occurrence, 55 Ultraviolet radiation (UVR), 102

absorption, 27

lens fiber absorption, 102 lifetime exposure, 105

overexposure (photokeratitis), 27b oxidative stress, relationship, 102 Unaccommodated ciliary ring, diameter

(decrease), 99b

Unaccommodated lens, refractive power, 93 Uncrossed retinal ganglion cell axons, course, 243f Unilateral ptosis, 164f

Unmyelinated nerve fibers, 6 passage, 234

Upper eyelids canaliculi, 178 extension, 160

lateral aspect, sensory fibers, 221 light micrograph, 167f meeting, 159

muscles, sensory fibers, 221 sagittal section, 163f sensory innervation, 221f

Uvea, 135–137

aging changes, 58–59 functions, 53–57 innervation, 57–58 sensory innervation, 57–58 structures, 1

tract, 40

Uveal blood vessels, 206f Uveal innervation, 57–58 Uveal meshwork, 97f

ropelike components, 95f Uveal tract, 40

blood supply, 57

V

Vascular choroid, nutrient supply, 57

Vascular endothelial growth factor (VEGF), 120 impact, 75–76

overproduction, 75–76 release, 28b

Vascular primary vitreous, 130f Veins, radial branches, 46f Venous branches, location, 214 Venous channel, 110

Venous sinus drainage, superior view, 216f

Ventral (anatomic direction), 3 Venules

formation, 134 joining, 52–53

Vergences (versions), 185 Vertebrate retinas, synaptic contacts

(arrangements), 73f Vertical rectus muscles, 192

Vidian nerve, pterygopalatine ganglion entry, 256 Visual-evoked response (VER), recordation, 144b Visual field, 5

defects, 246b

visual pathway, display, 247f

fiber orientation, relationship, 240–249 striate cortex, schematic, 250f

testing, 244b–245b

Visual information, striate cortex (combination), 239

Visual pathway

afferent pupillary light pathway, parallelism, 262 aging, 249–250

blood supply, 239–240 cells/synapses, 233 display, 247f

fibers, indication, 263f illustration, 234f second-order neuron, 66 structures, anatomy, 233–239 vascular pathway, 240f

Visual pigments activation, 79–80 location, 79

Visual system, 2f information collection, 1 specialization, 82–83

Vitamin A deficiency, 168b Vitreal attachments, 117 Vitreal function, 119 Vitreous, 138

presence, 62

Vitreous attachment, 117 Vitreous cells, location, 119 Vitreous chambers, 109, 117–120 Vitreous composition, 118–119 Vitreous cortex, 118

Vitreous physiology, 120 Vitreous production, 56

Vitreous structures, Eisner’s interpretation, 118f Vitreous zones, 117–118

Voltage-gated stimulants, 6–7 Voluntary muscle tissue, 6 Vortex veins, 52–53, 214

drainage, 214 formation, 135

W

Wake/sleep cycle, 83

Water movement, depiction, 25f

Water soluble alpha crystallins, decrease, 102–103 Whitnall’s ligament, 162

level, 191f

Wide-field amacrine cells (A17 cells), 69 Wing cells

formation, 136f light micrograph, 15f

Wing pairs, projection, 154b With-the-rule astigmatism, occurrence, 10b Wolfring, accessory lacrimal glands, 165

Y

Yoke muscles, 197 cardinal positions, 199f

Y sutures, 96–97

292

Index

 

 

 

 

 

 

 

 

Z

 

Zonular attachments, composite drawing, 96f

 

Zeis glands

Zonular fibers

 

development, 139

insertion, 93–94

 

duct, 165, 170

tertiary vitreous, stretching, 130f

 

location, 170f

Zonular lamella, 93–94

 

Zinn, zonules, 97

Zonular length, increase (absence), 99b

 

Zones of discontinuity, 103t

Zonule fibers, 47–48

 

Zonula adherens, 7

development, 138

 

terminal bars, 61–62

Zonules

 

Zonula occludens (ZO), 7

attachment point, 49f

 

barrier, loss, 25b–26b

lens, relationship (diagram), 94f

 

evidence, 134–135

Zonules of Zinn, 97

 

junctions, 11

Zygomatic bones, 148

 

completion, 12

Zygomatic nerve, 222

 

RPE cells, connection, 88

bypass, 256

 

terminal bars, 61–62

Zygomatic process, 144