Molecular genetic basis of sudden cardiac death

被引:21
作者
Towbin, JA
机构
[1] Texas Childrens Hosp, Dept Pediat Cardiol, Houston, TX 77030 USA
[2] Texas Childrens Hosp, Dept Cardiovasc Sci, Houston, TX 77030 USA
[3] Texas Childrens Hosp, Dept Mol & Human Genet, Houston, TX 77030 USA
[4] Baylor Coll Med, Houston, TX 77030 USA
关键词
D O I
10.1016/j.pcl.2004.04.012
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
This article outlines the up-to-date understanding of the molecular basis of disorders that cause sudden death. Several arrhythmic disorders that cause sudden death have been well-described at the molecular level, including the long QT syndromes and Brugada syndrome; this article reviews the current scientific knowledge of these diseases. Hypertrophic cardiomyopathy, a myocardial disorder that causes sudden death also has been well-studied. Finally, a disorder in which myocardial abnormalities and rhythm abnormalities coexist, arrhythmogenic right ventricular dysplasia, is described.
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收藏
页码:1229 / +
页数:28
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