Optic nerve Flashcards

1
Q

typical coloboma - location

A

inferonasal

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2
Q

typical coloboma is uni or bi

A

bi

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3
Q

Wallerian degeneration

A

(ascending atrophy) retrograde degeneration of axons (injury to the retina ganglion cells) toward the lateral geniculate body

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4
Q

descending atrophy

A

e.g. orbital tumor. atrophy toward the retinal genglion cells

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5
Q

mechanism of drusen formation

A

abnormal axonal metabolism leading to mitochondrial calcification

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6
Q

Tilted disc - uni or bi

A

Bi

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7
Q

Tilted disc - definition

A

oblique entry. ratio of the longest diameter to the shortest is >1.3

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8
Q

Tilted disc - complications

A

perimetry - superotemporal defects, OCT - sectoral RNFL thinning, CNV, sensory macular detachment

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9
Q

Torsional disc - definition

A

long axis is inclined at >15 st from the vertical meridian

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10
Q

Optic disc pit - VA, FAF, FA, complications

A

VA normal, FAF hyper, FA no, VF defects, 50% serous macular detachment 30yo

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11
Q

optic disc drusen - uni or bi

A

75% bi

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12
Q

optic disc drusen - associations

A

retinitis pigmentosa, angioid streaks, 90% in Alagile syndrome

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13
Q

optic disc drusen - complications

A

RNFL thinning, 75% VF defects, juxtapapillary CNV, VH, vascular occlusions

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14
Q

Coloboma - genetics

A

sporadic, but may AD PAX6

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15
Q

Coloboma - associations

A

CHARGE syndrome, Goldenhar syndrome, CNS abnormalities. iris/lens/chorioretinal coloboma, microphthalmos, microcornea

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16
Q

Morning glory disc - genetics

A

sporadic, but may PAX6

17
Q

Morning glory disc - uni or bi

A

uni

18
Q

Morning glory disc - associations

A

PVF, frontonasal dysplasia, mid-facial anomalies, basal encephalocele, pituitary insufficiency

19
Q

Morning glory disc - complications

A

serous retinal detachment 30%, CNV

20
Q

Optic disc hypoplasia - uni or bi

A

uni or bi

21
Q

Optic disc hypoplasia - definition

A

foveola-disc distance 3x disc, diminished number of nerve fibers

22
Q

Optic disc hypoplasia - causes

A

young maternal age, primiparity, maternal exposure to agents, double ring sign

23
Q

de Morsier syndrome - other name, features

A

septo-optic dysplasia. bilateral hypoplasia, absent septum pellucidum, corpus callosum dysgenesis, hypopituitarism

24
Q

Optic disc aplasia

A

absent or rudimentary

25
Q

Megalopapilla - uni or bi

A

bi

26
Q

Megalopapilla - definitions, OCT

A

> =2.1 mm horizontal or vertical, area >2.5mm2. OCT RNFL thinning, but GCC normal

27
Q

Optic disc dysplasia

A

deformed

28
Q

Papillorenal (renal-coloboma) syndrome - genetics

A

AD, PAX6

29
Q

Papillorenal (renal-coloboma) syndrome - definition

A

failure of angiogenesis, renal and optic disc dysplasia

30
Q

Peripapillary staphyloma

A

non-hereditary, VA markedly reduced, may local RD

31
Q

Peripapillary staphyloma - uni or bi

A

uni

32
Q

Secondary IIH

A

Vit. A, tetracyclines, contraceptive pills, SLE, Lyme, sleep apnea