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富克斯综合征的遗传方式。

Inheritance of Fuchs' combined dystrophy.

作者信息

Magovern M, Beauchamp G R, McTigue J W, Fine B S, Baumiller R C

出版信息

Ophthalmology. 1979 Oct;86(10):1897-923. doi: 10.1016/s0161-6420(79)35340-4.

Abstract

The inheritance pattern of Fuchs' combined corneal dystrophy is not confirmed. Published pedigrees fail to demonstrate a 50% segregation and sex ratio. They include no more than two generations of affected individuals and indicate a strong, female predilection. The pedigree we will present shows 16 affected persons in four generations. The ratio of affected to unaffected and men to women is 1:1. Penetrance is apparently 100%. Nine of the affected are under 50 years of age; four are subteen age. Light and electron micrographs of corneal tissue from three patients in three different generations are consistent with the diagnosis of Fuchs' dystrophy. Fuchs' dystrophy can therefore be established as a classic autosomal dominant pattern.

摘要

富克斯联合角膜营养不良的遗传模式尚未得到证实。已发表的家系未能显示出50%的分离率和性别比例。它们所包含的受影响个体不超过两代,且显示出明显的女性偏好。我们将展示的这个家系在四代中有16名受影响者。受影响与未受影响者以及男性与女性的比例均为1:1。外显率显然为100%。其中9名受影响者年龄在50岁以下;4名是青少年。来自三个不同世代的三名患者的角膜组织光镜和电镜照片与富克斯营养不良的诊断相符。因此,富克斯营养不良可被确定为典型的常染色体显性模式。

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