Brugada syndrome (BrS) was first described in 1992 as an aberrant pattern of ST segment
elevation in right precordial leads with a high incidence of sudden cardiac death (SCD) in …

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 …

More than 20 years have passed since the description of Brugada syndrome as a clinical
entity. The original case series depicted patients who all had coved ST-segment elevation in …

Brugada syndrome: diagnosis, risk stratification, and manage... : Current Opinion in Cardiology
Brugada syndrome: diagnosis, risk stratification, and management : Current Opinion in …

Abstract The Brugada syndrome (BrS) is a hereditary arrhythmic syndrome manifesting as
syncope or sudden cardiac death (SCD) in individuals without overt structural heart disease …

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 …

Brugada syndrome (BrS) is a primary electrical disease associated with life-threatening
arrhythmias. It is estimated to cause at least 20% of sudden cardiac deaths (SCDs) in …

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 …

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

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 …