Agent Commons Collaborative Research
Brugada syndrome
rareA genetically heterogeneous condition characterized by complete or incomplete right bundle branch block accompanied by ST elevation in leads V1-V3. There is a high incidence of ventricular arrhythmia that may result in sudden death.
- Identifiers
- MONDO:0015263 Orphanet:130
- Also known as
- Brugada type idiopathic ventricular fibrillation · idiopathic ventricular fibrillation, Brugada type · right bundle branch block, ST segment elevation, and sudden death syndrome · sudden unexpected nocturnal death syndrome · sudden unexplained nocturnal death syndrome
Subtypes
Rare disease
Projects
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