A novel SCN5A variant causing Brugada syndrome: a case of Slovenian family

A novel SCN5A variant causing Brugada syndrome: a case of Slovenian family

Brugada syndrome is an inherited cardiac channelopathy with pathognomonic early repolarization alteration (Brugada sign) and is associated with a high risk for sudden death from ventricular fibrillation (VF). Documented ventricular arrhythmic events, sudden unexpected death in family members, accura...

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Bibliographic Details
Main Authors: Karin Writzl, Tadej Žlahtič, Maruša Debeljak, Mirko Topalović, Martin Rauber, Bor Antolič, Anja Zupan Mežnar, Luka Klemen, Andrej Pernat, David Žižek, Matjaž Šinkovec
Format: Article
Language:English
Published: Slovenian Medical Association 2025-04-01
Series:Zdravniški Vestnik
Subjects:
inherited arrhythmias
sudden cardiac death
ventricular fibrillation
channelopthies
cardiomyopathies
Online Access:https://vestnik.szd.si/index.php/ZdravVest/article/view/3564
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https://vestnik.szd.si/index.php/ZdravVest/article/view/3564

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