The Brugada syndrome describes a subgroup of patients at risk for the occurrence of
ventricular fibrillation who have no definable structural heart disease associated with a right …

The Brugada syndrome is an inherited channelopathy that alters the main transmembrane
ion currents that constitute the cardiac action potential. These changes not only modify the …

Brugada Syndrome Our understanding of Brugada syndrome (BrS) has evolved since the
syndrome was first described in 1992. BrS is considered to be a primary inherited …

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 …

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 (BrS) is an inherited channelopathy characterized by an elevated
ST segment or J wave appearing in the right precordial leads (V1–V3), often followed by a …

In 1992 a new syndrome consisting of syncopal episodes and/or sudden death in patients
with a structurally normal heart and a characteristic electrocardiogram (ECG) with a pattern …

We report the case of a patient with genetically confirmed Brugada syndrome who presented
with ST-segment elevation in the right precordial and inferior leads. The presenting …

Brugada syndrome is a primary electrical disease of the heart that causes sudden cardiac
death or life‐threatening ventricular arrhythmias, especially in younger men. Genetic …

First described in 1992, Brugada syndrome is characterized by a specific
electrocardiographic pattern in the right precordial leads and susceptibility to ventricular …