中胚层发育不全：家族性虹膜异常。

Journal of pediatric ophthalmology Pub Date : 1977-11-01

J H Drouilhet, A I Arbisser, M L Mazow

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引用次数: 0

摘要

一个家族的前虹膜间质发育不全，无角度异常，无青光眼。家谱提示常染色体显性遗传模式。这与前房劈裂综合征的主要外周畸形和其他具有类似虹膜改变的疾病实体相比较。谱系代表中胚层发育不良或前房劈裂综合征连续体上的一个点。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

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Mesoectodermal dysgenesis: familial iris anomaly.

A family is described with hypoplasia of the anterior iris stroma, no angle anomalies, and no glaucoma. The pedigree is suggestive of an autosomal dominant mode of inheritance. This is compared to the main peripheral malformations of the anterior chamber cleavage syndrome and other disease entities with similar iris changes. The pedigree represents a point on the continuum of mesoectodermal dysgenesis or anterior chamber cleavage syndrome.

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Journal of pediatric ophthalmology

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