Paediatrics Flashcards
Visual acuity in a newborn
6/200-6/60
Visual acuity at 3 months
6/90-6/60
Visual acuity at 6 months
6/36-6/30
Visual acuity at 9 months
6/24
Visual acuity at 1 year
6/18
Visual acuity at 18 months
6/12
Visual acuity at 2 years
6/12-6/6
Which tools can be used to measure VA under 1 year?
keeler, teller or Cardiff cards - forced preferential looking
What tool is used to measure VA 6m-2y?
Cardiff pics
What tool is used to measure VA 2y-3y?
Kay pics
What tool is used to measure VA 3y-5y?
Sheridan-Gardiner
Crowded Kays
Why is infection more likely to spread to infect the orbit in children under 1y?
orbital septum not developed
What is the most common cause of orbital cellulitis in children? Where does the infection originate? (NOT WHAT BUG)
Ethmoidal sinus infection
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.
capillary haemangioma
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.
Optic nerve glioma
Valve at the junction of nasolacrimal sac and common canaliculus. Prevents reflux of tears.
Rosenmuller valve
Valve at the junction of the nasolacrimal duct and inferior nasal meatus. Prevents air entering the nasolacrimal duct during nose blowing.
Valve of Hasner
Baby under 1 y. Epiphora and mucopurulent discharge on pressure over the nasolacrimal sac. Not red. May resolve spontaneously.
Congenital nasolacrimal obstruction
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.
X-linked retinoschisis
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.
Stickler syndrome
Tx- 360 degree retinal laser
vitrectomy for RD
AD condition similar to Stickler syndrome but without systemic involvement. Low myopia, cortical cataract, empty vitreous and retinal detachment
Wagner syndrome
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.
Best’s Disease
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.
Stargardt disease
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
Lebers congenital amaurosis