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Ophthalmology · Conjunctiva and cornea: Peters anomaly
Sample itemA newborn has a dense central corneal opacity in both eyes. Slit lamp shows iris strands running from the collarette to the edge of the opacity, and a posterior corneal defect. What is the most likely diagnosis?
Original practice item, not a recalled exam question. Nothing here is recorded.
The answer and the reasoning
D. Peters anomaly
Peters anomaly is a central corneal leucoma with a defect of the posterior stroma, Descemet membrane and endothelium, with iris or lens adhesions to the back of the opacity. Glaucoma is a common associated problem, so it needs early assessment of pressure and visual rehabilitation.
Option by option
A. Sclerocornea
Sclerocornea is peripheral or total scleralisation of the cornea, without the central posterior defect and iris strands.
B. Congenital hereditary endothelial dystrophy
Congenital hereditary endothelial dystrophy gives diffuse ground-glass oedema, not a discrete central opacity with iris strands.
C. Axenfeld anomaly
Axenfeld anomaly has a prominent anterior Schwalbe line with peripheral iris strands, and the central cornea is clear.
D. Peters anomaly (correct)
Correct. A central opacity with a posterior corneal defect and iris adhesions defines Peters anomaly.
Source note: Original NextPrep sample item — pending expert review. This item is original practice material awaiting independent expert review, so confirm important facts in a standard textbook.
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