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.
Dokumententyp: | Zeitschriftenartikel |
---|---|
Fakultät: | Medizin |
Themengebiete: | 600 Technik, Medizin, angewandte Wissenschaften > 610 Medizin und Gesundheit |
ISSN: | 2193-5203 |
Sprache: | Deutsch |
Dokumenten ID: | 64830 |
Datum der Veröffentlichung auf Open Access LMU: | 19. Jul. 2019, 12:16 |
Letzte Änderungen: | 04. Nov. 2020, 13:44 |