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Variable expressivity of autosomal dominant microcornea with cataract.

作者信息

Salmon J F, Wallis C E, Murray A D

机构信息

Department of Ophthalmology, University of Cape Town, Groote Schuur Hospital, South Africa.

出版信息

Arch Ophthalmol. 1988 Apr;106(4):505-10. doi: 10.1001/archopht.1988.01060130551034.

Abstract

Autosomal dominant microcornea with a cataract, previously described in four families, was documented in a seven-generation family. Eighteen family members had microcornea and a cataract, and an additional six had sclerocornea or Peters' anomaly. Most individuals with microcornea had a corneal diameter of less than 11 mm in both meridians, with moderately steep corneal curvatures. The inherited cataract progressed to form a total cataract after visual maturity had been achieved. In the four affected children who had not undergone cataract extraction, the common abnormality was a posterior polar lens opacity. The variability of expressivity of the dominant gene would suggest that the embryological origins of microcornea and sclerocornea are similar.

摘要

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