Brugada syndrome in Iran: Insights from a 12‐year longitudinal study

Background Brugada syndrome (BrS) is characterized by ST‐segment elevation in the right precordial leads, which is not explained by ischemia, electrolyte disturbances, or obvious structural heart disease. Aim In present study, we aim to evaluate presentation, long‐term outcome, genetic findings, and...

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Veröffentlicht in:	Journal of cardiovascular electrophysiology 2024-04, Vol.35 (4), p.708-714
Hauptverfasser:	Haghjoo, Majid, Askarinejad, Amir, Madadi, Shabnam, Fazelifar, Amirfarjam, Kamali, Farzad, Alizadeh‐Diz, Abolfath, Emkanjoo, Zahra
Format:	Artikel
Sprache:	eng
Schlagworte:	Brugada syndrome Brugada Syndrome - diagnosis Brugada Syndrome - genetics Brugada Syndrome - therapy Defibrillators, Implantable Diagnosis EKG Electrocardiography Electrocardiography - methods Female genetic study Heart diseases Humans Iran Ischemia Longitudinal Studies long‐term outcome Male Mutation SCN5A gene Syncope Therapeutic applications
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