Brugada syndrome (BrS) is an inherited cardiac arrhythmia syndrome that causes a
heightened risk for ventricular tachyarrhythmias and sudden cardiac death. BrS is …

Background Brugada syndrome (BrS) is among the more common familial arrhythmia
syndromes, with an estimated prevalence of 1 to 5 per 10 000 persons. It is characterized by …

The Brugada syndrome (BS) is a hereditary disease characterized by typical
electrocardiographic alterations (elevation of the ST segment in right precordial leads) that …

Abstract In 1992, the Brugada syndrome (BrS) was recognized as a disease responsible for
sudden cardiac death, characterized by a right bundle-branch block with ST segment …

Brugada syndrome is a rare but serious inherited heart disease that causes sudden cardiac
death by polymorphic ventricular tachycardia or ventricular fibrillation. It is an autosomal …

Brugada syndrome (BS) is an inherited disease characterized by a coved-type ST-segment
elevation in the right precordial leads and increased risk of sudden cardiac death (SCD), in …

Brugada syndrome is a rare inherited arrhythmia syndrome leading to an increased risk of
sudden cardiac death, despite a structurally normal heart. Diagnosis is based on a specific …

Brugada syndrome (BrS) is a rare hereditary arrhythmia disorder, with a distinctive ECG
pattern, correlated with an increased risk of ventricular arrhythmias and sudden cardiac …

Brugada syndrome (BrS) is an inherited primary arrhythmia syndrome, first described in
1953 by Osher and Wolff, 1 and subsequently by several others including Martini and …

The Brugada syndrome (BrS) is an inherited channelopathy characterized by an elevated
ST segment or J wave appearing in the right precordial leads (V1–V3), often followed by a …