Background: BrS is an inherited sudden cardiac death syndrome. Less than 35% of BrS
probands have genetically identified pathogenic variants. Recent evidence has implicated …

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 …

Brugada syndrome, first described as a new clinical entity by Pedro and Josep Brugada in
1992, has attracted great interest because of its high prevalence in many regions of the …

Eighteen years2 after the initial description of 8 patients with what has become known as
Brugada syndrome, this disease has changed from an ECG curiosity to a diagnosis to be …

Brugada syndrome (BrS) is an inherited disease with an increased risk of sudden cardiac
death (SCD). However, testing identifies genetic disorders in only 20–30% of patients …

Introduction: The Brugada syndrome (BrS) is an inherited cardiac arrhythmia syndrome
characterized by prominent J waves appearing as distinct coved type ST segment elevation …

Background—Loss-of-function mutations in SCN5A have been associated with the Brugada
syndrome. We report the first Brugada syndrome family with compound heterozygous …

Background: Three types of characteristic ST-segment elevation are associated with
Brugada syndrome but only type 1 is diagnostic. Why only type 1 ECG is diagnostic remains …

Brugada syndrome (BrS) is primary electrical disorder characterized by ST segment
elevation with right bundle branch block morphology in patients with apparent structurally …

Background Brugada syndrome (BrS) is considered to be an inherited arrhythmic disease
associated with fatal complications and premature sudden unexpected death. The …