Brugada syndrome (BrS), is a primary electrical disorder predisposing affected individuals to
sudden cardiac death via the development of ventricular tachycardia and fibrillation (VT/VF) …

Brugada syndrome (BrS) is an inherited ion channel channelopathy predisposing to
ventricular arrhythmias and sudden cardiac death. Originally believed to be predominantly …

Brugada syndrome is a rare hereditary arrhythmia disorder characterized by a distinctive
electrocardiogram pattern and an elevated risk of ventricular arrhythmias and sudden …

After its recognition as a distinct clinical entity, Brugada syndrome is increasingly recognized
worldwide as an important cause of sudden cardiac death. Brugada syndrome exhibits …

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 (BS) is an inherited cardiac disorder characterized by typical
electrocardiographic patterns of ST segment elevation in the precordial leads, right bundle …

The Brugada syndrome is characterized by ST segment elevation in the right precodial
leads V1-V3 on surface ECG accompanied by episodes of ventricular fibrillation causing …

Abstract The Brugada syndrome (BrS) is an inherited arrhythmia characterized by ST‐
segment elevation in V1–V3 leads and negative T wave on standard ECG. BrS patients are …

Brugada syndrome (BrS) is a rare hereditary arrhythmia disorder, with a distinctive ECG
pattern, correlated with an increased risk of ventricular arrhythmias and sudden cardiac …

classified as an inherited channelopathy and has been linked to mutations in the SCN5A
gene that encodes the alpha subunit of the cardiac sodium channel (1). Patients with BrS …