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
收藏
页码：385 / 390
页数：6
相关论文
共 50 条
12345