Abstract
Inherited cardiac channelopathies are frequent causes of arrhythmogenic syncope and sudden cardiac death in young adults. When timely diagnosed and treated properly, they can be well controlled with anti-arrhythmic therapy and ICDs. Adequate risk stratification is crucial in the management of these diseases. As the individual arrhythmogenic risk can change over time, regular follow-ups are indicated. An increasing understanding of the genetic and pathophysiologic mechanisms of these diseases leads to the development of more targeted (mechanism-based) therapies.
Item Type: | Journal article |
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Faculties: | Medicine |
Subjects: | 600 Technology > 610 Medicine and health |
ISSN: | 2193-5203 |
Language: | German |
Item ID: | 64830 |
Date Deposited: | 19. Jul 2019, 12:16 |
Last Modified: | 04. Nov 2020, 13:44 |