ISSN 1016-5169 | E-ISSN 1308-4488
pdf
Recent Status in Brugada Syndrome [Turk Kardiyol Dern Ars]
Turk Kardiyol Dern Ars. 2022; 50(2): 137-144 | DOI: 10.5543/tkda.2022.21020

Recent Status in Brugada Syndrome

Fatih Bayrak1, Pedro Brugada2
1Department of Cardiology, Acıbadem Mehmet Ali Aydınlar University School of Medicine, İstanbul, Turkey
2Heart Rhythm Management Centre, UZ Brussel-VUB, Brussels, Belgium

Brugada syndrome was first described in 1992 as right precordial ST-segment elevation in patients with structurally normal hearts and sudden cardiac death. Brugada Syndrome is one of the most common reasons for sudden cardiac death (4-12%) and is a hereditary disease
with an autosomal dominant pattern of transmission with nearly 300 pathogenic variants in 19 responsible genes published. The present review focuses on the diagnosis, genetics, risk stratification, and management of patients with Brugada Syndrome.

Keywords: Arrhythmia, Brugada syndrome, sudden cardiac death

How to cite this article
Fatih Bayrak, Pedro Brugada. Recent Status in Brugada Syndrome. Turk Kardiyol Dern Ars. 2022; 50(2): 137-144

Corresponding Author: Fatih Bayrak
Manuscript Language: English


Journal Metrics

Journal Citation Indicator: 0.18
CiteScore: 1.1
Source Normalized Impact
per Paper:
0.22
SCImago Journal Rank: 0.348

Quick Search



Copyright © 2024 Archives of the Turkish Society of Cardiology



Kare Publishing is a subsidiary of Kare Media.