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法裔加拿大人家族中的诺里病:通过DNA分析检测携带者的尝试。

Norrie's disease in a French-Canadian kindred: attempt to detect carriers by DNA analysis.

作者信息

Polomeno R C, Zeesman S, MacDonald I M, Crozier D G, Tenniswood M P, Kaplan P

出版信息

Can J Ophthalmol. 1987 Feb;22(1):21-3.

PMID:3815151
Abstract

In a French-Canadian kindred four male cousins are affected with Norrie's disease, a rare X-linked recessive disorder. Three have university education, and the fourth has some developmental delay. Only one is microcephalic. All have mild to severe hearing deficit, although only three were aware of their hearing loss. Linkage analysis of DNA from family members with the probe L1.28 failed to detect female carriers.

摘要

在一个法裔加拿大人家族中,四名男性表亲患有诺里病,这是一种罕见的X连锁隐性疾病。其中三人接受过大学教育,第四人有一定程度的发育迟缓。只有一人患小头畸形。所有人都有轻度至重度听力缺陷,不过只有三人意识到自己听力丧失。用探针L1.28对家族成员的DNA进行连锁分析,未能检测到女性携带者。

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