CONGENITAL MUSCULAR-DYSTROPHIES

被引：25

作者：

ARAHATA, K ^{[1
]}

ISHII, H ^{[1
]}

HAYASHI, YK ^{[1
]}

机构：

[1] TOKYO METROPOLITAN HIGAHIYAMATO MED CTR HANDICAPP, TOKYO, JAPAN

来源：

CURRENT OPINION IN NEUROLOGY | 1995年 / 8卷 / 05期

关键词：

D O I：

10.1097/00019052-199510000-00011

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

Considerable advances in the understanding of congenital muscular dystrophy made during the past year may allow a new clinical classification of this disease. In particular, (1) evidence has accumulated to suggest that a laminin alpha2-chain (alpha2 subunit of laminin-2 or merosin) deficiency causes a type of congenital muscular dystrophy, and (2) it has been postulated that Fukuyama-type congenital muscular dystrophy and Walker-Warburg syndrome (but not Finnish muscle-eye-brain disease) are genetically identical diseases.

引用

页码：385 / 390

页数：6

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