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福山型先天性肌营养不良与沃克-沃尔堡综合征的基因同一性。

Genetic identity of Fukuyama-type congenital muscular dystrophy and Walker-Warburg syndrome.

作者信息

Toda T, Yoshioka M, Nakahori Y, Kanazawa I, Nakamura Y, Nakagome Y

机构信息

Department of Human Genetics, School of International Health, University of Tokyo, Japan.

出版信息

Ann Neurol. 1995 Jan;37(1):99-101. doi: 10.1002/ana.410370118.

Abstract

Both Fukuyama-type congenital muscular dystrophy (FCMD) and Walker-Warburg syndrome (WWS) are unusual genetic syndromes consisting of congenital muscular dystrophy and complex malformations of the brain and eye. It has been intensively discussed whether FCMD and WWS belong to the same disease entity or not. We analyzed a family in which 3 siblings were affected with either FCMD or WWS by using polymorphic microsatellites flanking the FCMD locus on chromosome 9q31-33. The results suggested that both FCMD and WWS siblings shared the identical combination of mutations on either allele of the FCMD locus. FCMD and WWS could be "genetically" identical.

摘要

福山型先天性肌营养不良(FCMD)和沃克-沃尔堡综合征(WWS)均为罕见的遗传综合征,其特征为先天性肌营养不良以及脑和眼的复杂畸形。FCMD和WWS是否属于同一疾病实体一直是人们深入讨论的话题。我们通过使用位于9号染色体q31 - 33上FCMD基因座侧翼的多态微卫星,对一个有3个兄弟姐妹患有FCMD或WWS的家庭进行了分析。结果表明,FCMD和WWS的患病兄弟姐妹在FCMD基因座的任何一个等位基因上都具有相同的突变组合。FCMD和WWS可能在“基因上”是相同的。

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