Introduction: First described in 1992 by the Brugada brothers, Brugada syndrome is
channelopathy of the sodium channels in the heart. It is a genetic disorder, over 60 different …

Brugada syndrome (BrS) is a rare disease, caused by mutations in the gene that encodes
cardiac sodium channel and is characterized by ST-segment elevation in the right precordial …

Brugada syndrome (BrS) is an autosomal-dominant condition mainly caused by defects in
sodium channels causing ST-segment elevation in electrocardiograms (ECGs) in the V1 and …

Background. Brugada syndrome was first described in 1992. Initially it was regarded as an
electrocardiographic curiosity, but in recent years the syndrome has been subject to great …

The Brugada Syndrome (BrS) is an inherited cardiac ion channel disorder associated with
increased risk of ventricular arrhythmias and mortality. Diagnosis is based on a …

The Brugada Syndrome (BrS) is an inherited cardiac ion channel disorder associated with
increased risk of ventricular arrhythmias and mortality. Diagnosis is based on a …

AIM: To evaluate the clinical characteristics of patients with diverse genetic variants of
Brugada syndrome. MATERIALS AND METHODS: 24 patients (17 male and 7 female) aged …

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 …

In the 18 years since the first description of Brugada Syndrome in a small series of cardiac
arrest survivors it has become evident that there is a marked spectrum in phenotype and …

Brugada syndrome is a genetic cause of sudden cardiac arrest characterized by abnormal
electrocardiographic (ECG) pattern in the right precordial leads either at rest or after …