The familial periodic paralyses and nondystrophic myotonias

被引：54

作者：

Ptácek, L ^{[1
]}

机构：

[1] Univ Utah, Howard Hughes Med Inst, Eccles Inst Human Genet 4420, Dept Neurol, Salt Lake City, UT 84112 USA

[2] Univ Utah, Howard Hughes Med Inst, Dept Human Genet, Salt Lake City, UT 84112 USA

来源：

AMERICAN JOURNAL OF MEDICINE | 1998年 / 105卷 / 01期

关键词：

D O I：

10.1016/S0002-9343(98)00123-5

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

There are two major categories of disease - hyperkalemic and hypokalemic periodic paralysis - each with mutations in a specific gene involving voltage-gated sodium or calcium channels. A variety of clinical presentations can occur, most of which can be treated successfully.

引用

页码：58 / 70

页数：13

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