Polymorphic catecholergic ventricular tachycardia [Supplementary Concept]
Condition where patients present with SYNCOPE and distinct stress-induced TACHYCARDIA without a prolonged QT-interval but heart is structurally normal. Onset occurs in childhood or adolescence and. Germline mutations in the RYR2 gene have been identified. OMIM: 180902
Date introduced: August 25, 2010
MeSH Unique ID: C536334
Heading Mapped to:
Entry Terms:
- Bidirectional Tachycardia Induced By Catecholamines
- Ventricular Tachycardia, Catecholaminergic Polymorphic, 1
- Catecholamine-induced polymorphic ventricular tachycardia
- Catecholaminergic polymorphic ventricular tachycardia
- Familial polymorphic ventricular tachycardia
- Ventricular Tachycardia, Familial Polymorphic
- Ventricular Tachycardia, Familial
- Stress-induced polymorphic ventricular tachycardia
- Cpvt2
- Ventricular Tachycardia, Catecholaminergic Polymorphic, 2