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Living with Catecholaminergic polymorphic ventricular tachycardia

A heart rhythm condition in which exercise or strong emotions can trigger a dangerously fast heartbeat.

Understanding Catecholaminergic polymorphic ventricular tachycardia

Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a condition that causes abnormal heart rhythms (arrhythmia).

When the heart rate rises with physical activity or emotional stress, it can trigger a very fast heartbeat called ventricular tachycardia. Episodes can cause light-headedness, dizziness, and fainting. They usually begin in childhood. If CPVT is not recognized and treated, an episode may cause the heart to stop beating (cardiac arrest).

Signs & symptoms

Symptoms vary from person to person. GARD lists these among the most common:

  • Dizzy spells
  • Pounding or racing heartbeat (palpitations)
  • Fainting (syncope)
  • Ventricular tachycardia (very fast heartbeat)
  • Atrial fibrillation (irregular upper-chamber beating)
  • Cardiac arrest (heart stops beating)

Not everyone has every symptom. GARD's list comes from the Human Phenotype Ontology.

Diagnosis

  1. Talk with your doctor

    Share the symptoms you've noticed, when they started and your family health history. Notes and photos can help.

  2. See a specialist

    Specialists who may be involved include genetic specialists and heart and blood vessel specialists.

  3. Ask which tests can help

    Your care team will decide which exams and tests can confirm the diagnosis.

  4. Connect with expert centers

    SADS Foundation may keep lists of experts for this condition.

Care & treatment

Care team
Genetic specialists (geneticists); Heart and blood vessel specialists (cardiologists)
Expert care
Expert lists: SADS Foundation
Treatment
GARD doesn't list specific treatments for this condition. Your care team will tailor care to your symptoms.
Research
Clinical trials and observational studies may be options. See the research section below.

General information, not medical advice. Your care team makes the decisions.

Everyday life

Living with a rare condition is easier with support.

  • Connect with SADS Foundation
  • Keep notes on symptoms, changes and questions for appointments
  • Ask about patient registries that help research
  • Look into financial aid and travel resources for care visits
Bring these questions to your next doctor visit
Can genetic testing find the cause in my family?
What activity limits or emergency plans do you advise?
Should my family members have heart screening?

Quick facts

Symptoms usually startfrom Childhood to Adulthood
InheritanceAutosomal Dominant, Autosomal Recessive

GARD says changes in genes cause CPVT. It may be inherited in an autosomal dominant way, where one changed gene copy can cause it, or in an autosomal recessive way, where a child gets a changed copy from each parent.

Genetic

Also known as: bidirectional tachycardia induced by catecholamine; bidirectional ventricular tachycardia induced by catecholamine; catecholamine-induced polymorphic ventricular tachycardia; cpvt; cvpt; double tachycardia induced by catecholamines

Patient organizations

  • SADS FoundationCatecholaminergic polymorphic ventricular tachycardia · United States
Source: NIH GARD · Catecholaminergic polymorphic ventricular tachycardiaGARD ID 4421 · GARD page updated September 2026 · Plain-language summary by Know Rare; editorial review pending. General information, not medical advice.

You are more than your diagnosis

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