Brugada syndrome.

doi:10.1186/1750-1172-1-35

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Article

Brugada syndrome.

Orphanet journal of rare diseases - 14 Sept 2006

Napolitano Carlo, Priori Silvia G

Abstract excerpt

A novel clinical entity characterized by ST segment elevation in right precordial leads (V1 to V3), incomplete or complete right bundle branch block, and susceptibility to ventricular tachyarrhythmia and sudden cardiac death has been described by Brugada et al. in 1992. This disease is now frequently called "Brugada syndrome" (BrS). The prevalence of BrS in the general population is unknown. The suggested...

Topics

Anti-Arrhythmia Agents
Brugada Syndrome
Defibrillators, Implantable
Humans
Muscle Proteins
Mutation
NAV1.5 Voltage-Gated Sodium Channel
Quinidine
Sodium Channels

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Identifiers

PMID: 16972995
DOI: 10.1186/1750-1172-1-35
PMCID: PMC1592481

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