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脊髓性肌萎缩症急性和慢性形式之间的基因同质性。

Genetic homogeneity between acute and chronic forms of spinal muscular atrophy.

作者信息

Gilliam T C, Brzustowicz L M, Castilla L H, Lehner T, Penchaszadeh G K, Daniels R J, Byth B C, Knowles J, Hislop J E, Shapira Y

机构信息

Department of Psychiatry, Columbia University, New York, New York.

出版信息

Nature. 1990 Jun 28;345(6278):823-5. doi: 10.1038/345823a0.

Abstract

The childhood-onset spinal muscular atrophies (SMAs) describe a heterogeneous group of disorders that selectively affect the alpha motoneuron. We have shown that chronic childhood-onset SMA (SMA II and III) maps to a single locus on chromosome 5q. Acute SMA (SMA Type I/Werdnig-Hoffmann/severe/infantile) is the main cause of heritable infant mortality. Mapping the acute SMA locus by conventional methods is complicated by the rapidly fatal course of the disease and its recessive mode of inheritance. We present here the typing of four inbred acute-SMA families with DNA markers on chromosome 5q and analysis of these together with acute families from our previous study to demonstrate genetic homogeneity between the acute and chronic forms of SMA. The data indicate that the acute SMA locus maps to chromosome 5q11.2-13.3. Two families seem unlinked to 5q markers, raising the possibility of genetic heterogeneity or disease misclassification within the acute and chronic family sets.

摘要

儿童期发病的脊髓性肌萎缩症(SMA)是一组异质性疾病,选择性地影响α运动神经元。我们已经表明,慢性儿童期发病的SMA(SMA II型和III型)定位于5号染色体q臂上的一个单一基因座。急性SMA(SMA I型/韦尼克-霍夫曼病/严重型/婴儿型)是遗传性婴儿死亡的主要原因。通过传统方法定位急性SMA基因座因疾病快速致命的病程及其隐性遗传模式而变得复杂。我们在此展示了四个携带5号染色体q臂上DNA标记的急性SMA近亲家系的分型,并将这些与我们之前研究中的急性家系一起进行分析,以证明急性和慢性SMA形式之间的遗传同质性。数据表明,急性SMA基因座定位于5q11.2 - 13.3。两个家系似乎与5q标记不连锁,这增加了急性和慢性家系组内遗传异质性或疾病分类错误的可能性。

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