Cardiac Ion Channel Diseases ("Channelopathies"): An Update

被引:0
|
作者
Dittmann, S. [1 ]
Stallmeyer, B. [1 ]
Mueller, J. [1 ]
Seebohm, G. [1 ]
Schulze-Bahr, E. [1 ]
机构
[1] Univ Klinikum Munster, Inst Genet Herzerkrankungen, Domagkstr 3, D-48149 Munster, Germany
关键词
ion channel diseases; Brugada syndrome; long QT syndrome; short QT syndrome; catecholaminergic polymorphic ventricular tachycardia; idiopathic ventricular fibrillation;
D O I
10.1055/s-0042-111903
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Cardiac ion channel diseases are rare diseases and are influenced by a variety of different genotypes. For the diagnosis molecular genetic studies are important because they allow a more precise classification. In the present review recent results of studies are summarized, illustrating the importance of molecular genetic analyses, and the necessity of long-term clinical studies in the field of ion channel diseases: long QT and short QT syndrome (LQTS and SQTS), Brugada syndrome (BrS), catecholaminergic polymorphic ventricular tachycardia (CPVT), and finally idiopathic ventricular fibrillation.
引用
收藏
页码:282 / 288
页数:7
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