Genetics of human partial epilepsy

被引:25
作者
Berkovic, SF
Scheffer, IE
机构
[1] UNIV MELBOURNE, AUSTIN & REPATRIAT MED CTR, DEPT MED NEUROL, HEIDELBERG, GERMANY
[2] ROYAL CHILDRENS HOSP, DEPT NEUROL, MELBOURNE, VIC, AUSTRALIA
关键词
D O I
10.1097/00019052-199704000-00007
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
A minor genetic predisposition to partial epilepsy has been long recognized. Recently, a group of idiopathic partial epilepsies with autosomal dominant inheritance has been identified. The clinical features and molecular genetic findings in these epilepsies are outlined in the present review. The first genetic defect in an idiopathic epilepsy has been found in autosomal dominant nocturnal frontal lobe epilepsy, the archetype of this newly recognized group of inherited partial epilepsies.
引用
收藏
页码:110 / 114
页数:5
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