Genetics reference · Cardiology

Arrhythmogenic right ventricular cardiomyopathy

MedlinePlus Genetics, National Library of Medicine · Retrieved 2026-10-13

Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a form of heart disease that usually appears in adulthood. ARVC is a disorder of the myocardium, which is the muscular wall of the heart. This condition causes part of the myocardium to break down over time, increasing the risk of an abnormal heartbeat (arrhythmia) and sudden death. ARVC may not cause any symptoms in its early stages. However, affected individuals may still be at risk of sudden death, especially…

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Reference details

Inheritance patterns
Autosomal dominant; Autosomal recessive
Other names
Arrhythmogenic right ventricular cardiomyopathy-dysplasia; Arrhythmogenic right ventricular dysplasia; Arrhythmogenic right ventricular dysplasia/cardiomyopathy; ARVC; ARVD; ARVD/C; Right ventricular dysplasia, arrhythmogenic; Ventricular dysplasia, right, arrhythmogenic
NLM review date
2010-05
NLM publication date
2020-08-18

Description

Arrhythmogenic right ventricular cardiomyopathy (ARVC) is a form of heart disease that usually appears in adulthood. ARVC is a disorder of the myocardium, which is the muscular wall of the heart. This condition causes part of the myocardium to break down over time, increasing the risk of an abnormal heartbeat (arrhythmia) and sudden death. ARVC may not cause any symptoms in its early stages. However, affected individuals may still be at risk of sudden death, especially during strenuous exercise. When symptoms occur, they most commonly include a sensation of fluttering or pounding in the chest (palpitations), light-headedness, and fainting (syncope). Over time, ARVC can also cause shortness of breath and abnormal swelling in the legs or abdomen. If the myocardium becomes severely damaged in the later stages of the disease, it can lead to heart failure.

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Source date: 2010-05. Retrieved: 2026-10-13. Text has been organized for reading; this import has not been independently reviewed by a clinician. It is not individualized medical advice.
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