Brugada syndrome is an inherited disease characterized by an increased risk of sudden
cardiac death owing to ventricular arrhythmias in the absence of structural heart disease …

The Brugada syndrome is an inherited disorder associated with risk of ventricular fibrillation
and sudden cardiac death in a structurally normal heart. Diagnosis is based on a …

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 an inherited cardiac disorder, characterised by a typical ECG
pattern and an increased risk of arrhythmias and sudden cardiac death (SCD). BrS is a …

Brugada syndrome is characterized by ST-segment elevation in the right precordial leads
(V1–V3) and an episode of ventricular fibrillation (VF) in the absence of structural heart …

Brugada syndrome is an inherited arrhythmogenic disorder, characterised by coved-type ST-
segment elevation in the right precordial leads, and is associated with increased risk of …

Until recently, the cellular basis for sudden death, the Brugada Syndrome, has largely
remained an unknown to modern arrhythmologists and cardiologists, particularly in the …

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 …

Since its first description in 1992 as a new clinical entity, the Brugada syndrome has
aroused great interest among physicians and basic scientists. Two consensus conferences …

In 1992, Brugada and Brugada introduced a new clinical entity characterized by right
precordial ST-segment elevation followed by a negative T-wave and a high incidence of …