Paediatrics Flashcards

1
Q

Visual acuity in a newborn

A

6/200-6/60

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2
Q

Visual acuity at 3 months

A

6/90-6/60

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3
Q

Visual acuity at 6 months

A

6/36-6/30

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4
Q

Visual acuity at 9 months

A

6/24

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5
Q

Visual acuity at 1 year

A

6/18

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6
Q

Visual acuity at 18 months

A

6/12

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7
Q

Visual acuity at 2 years

A

6/12-6/6

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8
Q

Which tools can be used to measure VA under 1 year?

A

keeler, teller or Cardiff cards - forced preferential looking

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9
Q

What tool is used to measure VA 6m-2y?

A

Cardiff pics

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10
Q

What tool is used to measure VA 2y-3y?

A

Kay pics

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11
Q

What tool is used to measure VA 3y-5y?

A

Sheridan-Gardiner

Crowded Kays

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12
Q

Why is infection more likely to spread to infect the orbit in children under 1y?

A

orbital septum not developed

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13
Q

What is the most common cause of orbital cellulitis in children? Where does the infection originate? (NOT WHAT BUG)

A

Ethmoidal sinus infection

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14
Q

Baby 2 months-1 year. Unilateral asymmetrical raised bright red lesions most commonly in the upper eyelid which may obscure visual axis and cause ambylopia. If deep can cause axial proptosis. Lesions blanches on pressure and enlarges on crying.

A

capillary haemangioma

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15
Q

Gradual painless, monocular decrease in visual acuity with RAPD. Non-axial proptosis. CT head shows fusiform enlargement of optic nerve. Cafe au lait spots, lisch nodules and axillary freckling.

A

Optic nerve glioma

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16
Q

Valve at the junction of nasolacrimal sac and common canaliculus. Prevents reflux of tears.

A

Rosenmuller valve

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17
Q

Valve at the junction of the nasolacrimal duct and inferior nasal meatus. Prevents air entering the nasolacrimal duct during nose blowing.

A

Valve of Hasner

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18
Q

Baby under 1 y. Epiphora and mucopurulent discharge on pressure over the nasolacrimal sac. Not red. May resolve spontaneously.

A

Congenital nasolacrimal obstruction

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19
Q

Hypermetropic boys with reading difficulties due to splitting of the retina at the nerve fibre layer. Bilateral maculopathy, foveal schisis with spoke-like folds resembling CMO. Scotopic ERG.

A

X-linked retinoschisis

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20
Q

AD condition causing defect in type 2 collagen, leading to retinal detachment (50%). High myopia, cataract, ectopia lentis, glaucoma, empty vitreous. Sensorineural hearing loss. Pierre robin or marfanoid features.

A

Stickler syndrome

Tx- 360 degree retinal laser
vitrectomy for RD

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21
Q

AD condition similar to Stickler syndrome but without systemic involvement. Low myopia, cortical cataract, empty vitreous and retinal detachment

A

Wagner syndrome

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22
Q

AD condition in hypermetropic patients. Bilateral macular degeneration, lipofuscin accumulation in the RPE and atrophy of the photoreceptor layer of the retina. Egg yolk lesion at the macula. Abnormal EOG- decreased arden ratio.

A

Best’s Disease

23
Q

AR condition due to mutation in ABCA4 gene on chromosome 1. Most common inherited macular dystrophy. Beaten bronze macula progressing to bullseye pattern. Pisciform yellow/white lesions in RPE. Dark choroid due to reduced choroidal circulation.

A

Stargardt disease

24
Q

AR condition with severe visual loss at birth, nystagmus, roving eye movements and absent pupillary reflexes and oculodigital syndrome. Associated with hypermetropia. Salt and pepper retinopathy

A

Lebers congenital amaurosis

25
Can be AD, AR or XL. Mutation in rhodopsin gene on chromosome 3. Dysfunction of rods then cones and degeneration of retinal tissue. Nyctalopia and tunnel vision. Pale waxy disc, bony spicules and arteriolar attenuation.
Retinitis pigmentosa
26
AR. Retinitis pigmentosa, bulls eye maculopathy, polydactyly, learning disability and obesity.
Badet-Biedl syndrome
27
AR. Retinitis pigmentosa and hearing loss. Most common inherited cause of deaf-blind.
Usher's syndrome
28
AR. Accumulation of phytanic acid. Retinitis pigmentosa, anosmia, peripheral neuropathy and ichthyosis (scaly skin)
Refsum syndrome
29
AR. Abnormal absorption of fat soluble vitamins. Retinitis pigmentosa, spinocerebellar ataxia, acanthocytosis.
Bassen Kornzweig syndrome
30
Conditions associated with leukocoria
``` congenital cataract retinoblastoma persistent fetal vasculature retinopathy of prematurity Coat's Disease toxicarias ```
31
Most common intraocular malignancy in children arising from embryonal photoreceptor cells. Associated with a mutation in Rb1 gene on chromosome 13. Flexner rosettes and Homer Wright rosettes and fleurettes.
retinoblastoma
32
Is Rb1 a tumour suppressor or oncogene?
tumour supressor
33
prem baby presents age 7 days with unilateral leukocoria, micro-ophthalmia and cataract
persistent foetal vasculature
34
baby born at 30 weeks gestation weighing 800g, required oxygen therapy for respiratory distress
retinopathy of prematurity
35
What is the end stage of retinopathy of prematurity?
total retinal detachment
36
what additional signs (Plus disease) may be present in ROP that can increase severity of the condition?
increased venous dilatation | arteriolar tortuosity of the peripheral retina
37
congenital condition affecting young boys. decreased visual acuity, strabismus and leukocoria. temporal retinal telangectasia and microaneurysms. can result in exudative retinopathy.
Coat's disease
38
Increase in innervation of a muscle is accompanies by a decrease in innervation of its antagonist. i.e. when lateral rectus contracts, medial rectus relaxes
Sherrington's law
39
what are yolk muscles?
muscles pulling the eyes in the same direction e.g. right LR and left MR
40
Yolk muscles have equal and simultaneous flow and innervation
Hering's law
41
developmental defect of spatial visual processing that can occur in the central visual pathway during the early years of life, leading to diminished vision. Causes include: stabismus, anisometropia and stimulus deprivation
Amblyopia
42
What pharmacological intervention can be used in amblyopia?
penalisation of good eye using atropine
43
In turning squint associated with hypermetropia. normal AC/A ratio
accommodative esotropia correct hypermetropia
44
in turning squint for near vision only. high AC/A ratio
convergence excess esotropia treat with bifocals or bilateral medial rectus recession
45
Non-accommodative in turning squint in child at 6 months. Large angle deviation and alternating fixation. Latent horizontal nystagmus.
infantile esotropia
46
out .turning squint associated with myopia. most common type
intermittent exotropia correct myopia
47
constant large angle out turning squint in baby at 6 months. associated with neurological abnormalities
constant exotropia
48
What nervous anomaly is seen in Duane retraction syndrome?
lateral rectus supplied by CN III
49
Deaf patient with globe retraction on adduction. Esotropia with limited abduction.
Duane retraction syndrome
50
Superior oblique restricted at trochlea. Globe sitting down and in. Limited elevation in adduction or on upgaze with associated click sensation.
Brown syndrome
51
resection vs recession
``` resection = shortening muscle to strengthen recession = loosening muscle to weaken ```
52
is strabismus concomitant?
yes, looks the same regardless of where you are looking
53
is CN III palsy concomitant?
no