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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

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