The Brugada syndrome is an inherited cardiac disorder initially described in 1992 by Pedro
and Josep Brugada, with variable electrocardiographic features characteristic of right bundle …

Brugada syndrome is characterized clinically by the onset of syncopes or sudden death
related to ventricular tachyarrhythmias in patients with a structurally normal heart. Its …

The number of scientific publications dealing with the syndrome has continued to increase
substantially in recent years. New polymorphisms, mutations and genes associated with the …

Brugada syndrome (BrS) is a hereditable syndrome, first reported in 1992, characterized by
right bundle branch block and an uncommon form of ST-T wave elevation in the V1 and V2 …

First introduced as a new clinical entity in 1992, the Brugada syndrome is associated with a
relatively high risk of sudden death in young adults, and occasionally in children and infants …

Brugada syndrome is electrocardiographically characterised by ST segment elevation in
right precordial leads and the occurrence of episodes of polymorphic ventricular …

Brugada syndrome is characterized clinically by the onset of syncopes or sudden death
related to ventricular tachyarrhythmias in patients with a structurally normal heart. Its …

A diagnostic triad characterizes Brugada syndrome. It consists of a right bundle branch
block, ST-segment elevation in leads V1-V3 and sudden cardiac death (SCD) …

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 …

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