The ABC's of limb-girdle muscular dystrophy:: α-sarcoglycanopathy, Bethlem myopathy, calpainopathy and more

被引：15

作者：

Gordon, ES ^{[1
]}

Hoffman, EP ^{[1
]}

机构：

[1] Childrens Natl Med Ctr, Med Genet Res Ctr, Washington, DC 20010 USA

来源：

CURRENT OPINION IN NEUROLOGY | 2001年 / 14卷 / 05期

关键词：

D O I：

10.1097/00019052-200110000-00004

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

Limb-girdle muscular dystrophy is a class of disorders encompassing many forms of this disease. Variation exists between the inheritance patterns, genes responsible, course of disease and symptoms, with the cohesive factor among these disorders being the predominance of proximal muscle weakness. Here we review each form of limb-girdle muscular dystrophy with attention to molecular genetics, clinical features, inheritance, and diagnostic issues pertaining to each primary genetic cause. Curr Opir Neurol 14:567-573. (C) 2001 Lippincott Williams & Wilkins.

引用

页码：567 / 573

页数：7

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