Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC)

Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC) is a rare heart disease. Learn causes, symptoms, treatment, and tips for managing daily life.

11 September, 2025

Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC) affects the heart’s rhythm and structure. Discover key signs, causes, and treatment options to stay informed.

What are the main causes of Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC)?

Genetic mutations in desmosomal proteins weaken the heart’s structure, leading to progressive right ventricular dysfunction and abnormal electrical signaling.
Family history of ARVC significantly raises risk, highlighting the strong hereditary influence of this rare but dangerous cardiac disorder.
Inflammatory responses and fibrosis replace healthy heart tissue with scar and fat, disrupting rhythm and causing dangerous arrhythmias.

ARVC symptoms include palpitations and fainting

>>> See more: Understanding Endocarditis (leading to valve damage) risks

Key symptoms of Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC) to watch for

Palpitations and irregular heartbeats often occur during exercise, signaling abnormal electrical activity within the right ventricle.
Episodes of fainting or dizziness result from reduced blood flow to the brain due to severe arrhythmias.
Sudden cardiac arrest may develop in advanced stages, especially in young athletes during physical exertion.

How can you prevent Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC) effectively?

Genetic screening for at-risk individuals helps identify ARVC early and enables timely medical intervention.
Regular cardiac monitoring detects rhythm abnormalities before they escalate into life-threatening complications.
Avoiding intense exercise lowers stress on the right ventricle, reducing risk of dangerous arrhythmias and sudden cardiac death.

Arrhythmogenic Right Ventricular Cardiomyopathy treatment uses meds, ICD, or ablation

>>> See more: Symptoms and warning signs of dilated cardiomyopathy (DCM)

Images visual examples of Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC)

Visual examples often show scarring and structural changes in the heart wall, helping illustrate how the condition disrupts both pumping function and electrical signaling.

Arrhythmogenic Right Ventricular Cardiomyopathy diagnosis uses ECG, MRI, and genetics

ARVC genetics often involve mutations in desmosomal proteins

Arrhythmogenic Right Ventricular Cardiomyopathy and exercise can trigger dangerous rhythms

Arrhythmogenic Right Ventricular Cardiomyopathy ICD prevents sudden cardiac death

ARVC patient stories show daily struggles

ARVC sudden death is a major concern

ARVC research explores new treatments

>>> See more: Symptoms and diagnosis of Hypertrophic Cardiomyopathy (HCM)

Managing Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC) requires awareness of symptoms, timely diagnosis, and proper treatment to maintain heart health.