Brugada syndrome (BS) is a genetic cardiac syndrome first described in 1992 that is
characterized by distinct abnormalities noted in leads V1 and V2 on electrocardiogram. It …

Electrocardiographic abnormalities constitute the hallmark of Brugada syndrome, and these
changes could be often dynamic. Differentiation between Brugada syndrome and other …

Brugada syndrome (BS) is an under recognized condition inherited through autosomal
dominant transmission that consists mainly of characteristic electrocardiogram findings with …

Brugada syndrome is an aberrant ST-segment elevation in the right precordial leads. It can
progress into sudden cardiac death (SCD) among patients with structurally normal hearts …

Brugada syndrome is an arrhythmogenic disease characterized by a pattern of ST segment
elevation in the right precordial leads on an electrocardiogram with an increased risk of …

Abstract In 1992, Brugada and Brugada described 8 patients with a history of aborted
sudden death and a distinct ECG pattern of right bundle-branch block with ST segment …

[1] Martini B, Cannas S, Nava A. Brugada by any other name. Eur Heart J 2001; 22: 1835–
7.[2] Brugada P, Brugada J. Right bundle branch block, persistent ST segment elevation and …

Background Brugada syndrome is a rare condition causing sudden death in young adults
due to unexpected sudden-onset ventricular fibrillation. Diagnosis is based on the presence …

Since its introduction as a clinical entity in 1992, the Brugada syndrome has progressed
from being a rare disease to one that is second only to automobile accidents as a cause of …

Brugada Syndrome and Supraventricular Tachyarrhythmias. Introduction: The Brugada
syndrome is a distinct form of idiopathic ventricular fibrillation characterized by a unique …