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

来源：

AKTUELLE KARDIOLOGIE | 2016年 / 5卷 / 04期

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

页码：282 / 288

页数：7