Ophthalmology Flashcards

1
Q

Causes of leukocoria

A
  • Congenital cataract
  • Retinoblastoma
  • Persistent fetal vasculature
  • Coats disease
  • Retinopathy of prematurity
  • Optic disc abnormalities
  • Uveitis
  • Toxocariasis
  • Coat’s disease
  • Norrie disease
  • Vitreous hemorrhage
  • Hereditary retinal dysplasia
  • Astrocytic hamartoma
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2
Q

Where is the lesion in a homonymous hemianopia?

A
  • incongruous defects: lesion of optic tract
  • congruous defects: lesion of optic radiation or occipital cortex
  • macula sparing: lesion of occipital cortex
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3
Q

Where is the lesion in a homonymous quadrantanopia?

A
  • superior: lesion of temporal lobe
  • inferior: lesion of parietal lobe
  • mnemonic = PITS (Parietal-Inferior, Temporal-Superior)
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4
Q

Where is the lesion in a bitemporal hemianopia?

A
  • lesion of optic chiasm
  • upper quadrant defect > lower quadrant defect = inferior chiasmal compression, commonly a pituitary tumour
  • lower quadrant defect > upper quadrant defect = superior chiasmal compression, commonly a craniopharyngioma
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5
Q

Extraocular muscle most at risk in orbital floor fracture?

A

Inferior rectus

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6
Q

Causes of corneal opacity

A
  • S - Sclerocornea
  • T - Tears in the Descemet membrane (can be due to birth trauma or congenital glaucoma)
  • U - Ulcers
  • M - Metabolic
  • P - Peters anomaly (abnormal development of the anterior segment)
  • E - oEdema
  • D Dermoid
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7
Q

Features of juvenile optic atrophy

A
  • Autosomal dominant inheritance
  • Bilateral
  • Symptoms start in early childhood
  • Severity of the vision loss varies widely between children
  • There is reduction in visual acuity, a pale optic disc, loss of color vision, and centrocecal scotomas
  • The symptoms occur due to atrophy of ganglion cells in the retina
  • There is also associated loss of myelin sheaths in the optic nerve.
  • The condition is often progressive
  • Irreversible process, but steroids are used to slow progresion
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8
Q

Eye features of Down’s

A
  • Watering eyes
  • Squint 20%
  • Hypermetropia 40%
  • Myopia 14%
  • Astigmatism 30%
  • Nystagmus 10%
  • Brushfield spots up to 90%
  • Cataracts
  • Keratoconus
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9
Q

Causes of coloboma

A
  • CHARGE (coloboma, heart anomaly, choanal atresia, restriction of growth/developement, genital anomaly, ear abnormality
  • In association with renal abnormalities
  • Cat eye syndrome
  • DiGeorge syndrome
  • Treacher Collins syndrome
  • Epidermal naevus syndrome
  • Velo-cardiofacial syndrome
  • Wolf-Hirschhorn syndrome
  • Kabuki syndrome
  • Goldenhar syndrome
  • MIDAS syndrome (microphthalmia, dermal aplasia, and sclerocornea)
  • Trisomy 21, 13, & 18
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10
Q

Features of retinoblastoma

A
  • Embryonal tumour of the eye
  • Most common under age 3
  • Majority are unilateral
  • Bilateral disease nearly always has a genetic component
  • Most commonly presents with strabismus or leukocoria
  • Treatment may be with photocoagulation, cryotherapy, radiotherapy, chemotherapy, or enucleation
  • The five-year survival in the UK is currently > 95%
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11
Q

What is the Hirschberg test for?

A

Squint

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