Polymorphic catecholergic ventricular tachycardia

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

Also Known As:

Bidirectional Tachycardia Induced By Catecholamines; Catecholamine-induced polymorphic ventricular tachycardia; Catecholaminergic polymorphic ventricular tachycardia; Cpvt2; Familial polymorphic ventricular tachycardia; Stress-induced polymorphic ventricular tachycardia; Ventricular Tachycardia, Catecholaminergic Polymorphic, 1; Ventricular Tachycardia, Catecholaminergic Polymorphic, 2; Ventricular Tachycardia, Familial; Ventricular Tachycardia, Familial Polymorphic

Cardiovascular Diseases: 94258
- Heart Diseases: 26486
  - Cardiac Arrhythmias: 21201
    - Tachycardia: 15935
      - Ventricular Tachycardia: 12821
        Polymorphic catecholergic ventricular tachycardia: 539
  - Cardiac Conduction System Disease: 95
    - Tachycardia: 15935
      - Ventricular Tachycardia: 12821
        Polymorphic catecholergic ventricular tachycardia: 539
Signs and Symptoms Pathological Conditions
- Pathologic Processes: 10385
  - Cardiac Arrhythmias: 21201
    - Tachycardia: 15935
      - Ventricular Tachycardia: 12821
        Polymorphic catecholergic ventricular tachycardia: 539

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Disease

Drug/Important Bio-Agent (IBA)