Molecular Mechanisms of Inherited Ventricular ArrhythmiasMolekulare Mechanismen angeborener ventrikulärer Arrhythmien

被引:0
|
作者
Thomas Wichter
Eric Schulze-Bahr
Lars Eckardt
Matthias Paul
Bodo Levkau
Matthias Meyborg
Michael Schäfers
Wilhelm Haverkamp
Günter Breithardt
机构
[1] Department of Cardiology and Angiology,
[2] University of Münster,undefined
[3] Germany,undefined
[4] Institute for Arteriosclerosis Research,undefined
[5] University of Münster,undefined
[6] Germany,undefined
[7] Department of Nuclear Medicine,undefined
[8] University of Münster,undefined
[9] Germany,undefined
关键词
Key Words: Ion channel; Gene mutation; Cardiomyopathy; Long QT syndrome; Brugada syndrome; Sudden death; Tachyarrhythmias; Ventricular tachycardia; Schlüsselwörter: Ionenkanal; Genmutation; Kardiomyopathie; QT-Syndrom; Brugada-Syndrom; Plötzlicher Herztod; Tachyarrhythmie; Ventrikuläre Tachykardie;
D O I
10.1007/s00059-002-2436-x
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学科分类号
摘要
Inherited ventricular arrhythmias such as the long QT syndrome (LQTS), Brugada syndrome, catecholaminergic polymorphic ventricular tachycardia (CPVT), idiopathic ventricular fibrillation (VF), and arrhythmogenic right ventricular cardiomyopathy (ARVC) account for a relevant proportion of sudden cardiac death cases in young patients cohorts. The detailed pathogenetic mechanisms of inherited ventricular arrhythmias are still poorly understood because systematic investigations are difficult to perform due to low patient numbers and the lack of appropriate experimental models. However, recent advances in research and science have identified a genetic background for many of these diseases.
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页码:712 / 739
页数:27
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