Abstract
Reporting a family in which a father and his 3 sons were diagnosed as Axenfeld- Rieger anomaly. Slit lamp evaluation showed bilateral megalocornea, posterior embryotoxon, corectopia. All had grade 2-3 RAPD, raised intraocular pressure with increased cup/disc ratio and tubular vision. On gonioscopy angles were open with peripheral iris strands. OCT revealed thinned out retinal nerve fiber layer. No other systemic manifestations were noticed. Thus reporting a family of Axenfeld-Rieger anomaly.
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Schedule a callMore From: Journal of Evolution of Medical and Dental sciences
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