Genetics of Brugada, long QT, and arrhythmogenic right ventricular dysplasia syndromes

被引:7
|
作者
Towbin, JA
Vatta, M
Li, H
机构
[1] Baylor Coll Med, Dept Pediat Cardiol, Houston, TX 77030 USA
[2] Texas Childrens Hosp, Dept Pediat Cardiol, Houston, TX 77030 USA
[3] Texas Childrens Hosp, Dept Cardiovasc Sci, Houston, TX 77030 USA
[4] Texas Childrens Hosp, Dept Mol & Human Genet, Houston, TX 77030 USA
关键词
long QT syndrome; Brugada syndrome; idiopathic ventricular fibrillation; ion channels; sodium channel; potassium channel; arrhythmogenic right ventricular dysplasia;
D O I
10.1054/jelc.2000.20361
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
This article outlines the up-to-date understanding of the molecular basis of primary ventricular arrhythmias. Two disorders have recently been well described at the molecular level, the long QT syndromes and Brugada syndrome, and this article reviews the current scientific knowledge of each disease. A third disorder, arrhythmogenic right ventricular dysplasia, which is on thc cusp of understanding, will also be described.
引用
收藏
页码:11 / 22
页数:12
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