Genetics of the febrile seizure susceptibility trait

被引:28
作者
Kugler, SL
Johnson, WG
机构
[1] Univ Med & Dent New Jersey, Robert Wood Johnson Med Sch, Dept Neurol, Piscataway, NJ 08854 USA
[2] Univ Med & Dent New Jersey, Robert Wood Johnson Med Sch, Dept Pediat, Piscataway, NJ 08854 USA
关键词
febrile seizures; genetics; linkage analysis; human chromosome 8; human chromosome 19;
D O I
10.1016/S0387-7604(98)00020-5
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Febrile seizures are the commonest form of convulsion, occurring in 2-5% of infants in Europe and North America and 6-9% of infants in Japan. In large families, the febrile seizure susceptibility trait is inherited by the autosomal dominant pattern with reduced penetrance. In the other families, inheritance appears to be multifactorial. Recent linkage studies provide evidence that regions of chromosomes 8 and 19 contain febrile convulsions (FC) susceptibility genes. This opens up the way tb cloning a febrile seizure gene and determining the contributions of these gene loci to febrile seizures in the sporadic cases and the small families. Cloning a febrile seizure gene will make possible new approaches to prevention and therapy. It will also be possible to determine whether a febrile seizure gene contributes to other types of seizures. (C) 1998 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:265 / 274
页数:10
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