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
收藏
页码：58 / 70
页数：13
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