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Arrhythmogenic Right Ventricular Dysplasia 2 C1832931

Published: July 22, 2026Updated: August 25, 2026

An inherited disorder where fatty tissue replaces the heart muscle in the right ventricle, leading to abnormal heart rhythms. It commonly affects young adults and may cause fainting or cardiac arrest. Treatment involves medications, catheter ablation, and ICD placement to control heart rhythm and prevent complications.

Medically reviewed by WellAlly Editorial TeamLast reviewed August 25, 2026Editorial policy

Key facts at a glance

ICD-10
I78.0
ICD-11
BA00.0
Body system
cardiovascular
Severity
severe
Chronic
true

Signs and symptoms

Common signs and symptoms that may indicate this condition.

Warning signs - seek immediate care

!

Chest pain

Chest discomfort or palpitations

(cardiovascular)

Significant symptoms that substantially affect daily functioning.

Frequency: Common at all stages

Heart palpitations

(cardiovascular)

Dyspnea on exertion

(cardiovascular)

Exercise intolerance

(cardiovascular)

Diagnosis and tests

How this condition is diagnosed and what test results mean.

Initial screening tests

1

Standard diagnostic workup

Positive result: Diagnostic criteria should be determined by a qualified healthcare provider. [Content pending medical review.]

Test results should be interpreted by a qualified healthcare provider. [Content pending medical review.]

Treatment options

Evidence-based approaches to managing this condition.

First-line treatments

1

Disease management and monitoring

Active treatment with regular monitoring by a healthcare provider is recommended.

medication
2

Beta-blocker Therapy

Foundation antiarrhythmic therapy using cardioselective or non-selective beta-blockers to reduce risk of exercise-induced arrhythmias and slow disease progression by decreasing right ventricular wall stress.

medication
3

ICD Placement for Secondary Prevention

Permanent defibrillator system for ARVD2 patients with prior cardiac arrest, documented sustained VT, or severe arrhythmic manifestations. Provides life-saving therapy for malignant ventricular arrhythmias.

procedure

Additional treatment options

Supervised Cardiac Rehabilitation

Structured exercise program under cardiac supervision with telemetry monitoring to maintain cardiovascular fitness within safe parameters while avoiding excessive RV strain from high-intensity activities.

physical_therapy

Adjunctive Antiarrhythmic Agents

Addition of Class III agents such as sotalol or amiodarone when beta-blocker monotherapy insufficient for arrhythmia control. Amiodarone reserved for refractory cases due to toxicity profile requiring regular monitoring.

medication

Genetic Testing and Family Screening

Comprehensive genetic evaluation for pathogenic desmoglein-2 and desmocollin-2 mutations with cascade family testing. Includes clinical screening with ECG, echocardiography, and MRI for at-risk relatives.

monitoring

When to seek medical help

Recognize when you need immediate medical attention.

See a doctor within 24 hours

Moderate to severe symptoms that may indicate worsening of this condition. Prompt medical evaluation is recommended.

Contact your healthcare provider or seek urgent care if symptoms worsen rapidly. Go to the emergency department for life-threatening symptoms.

Frequently asked questions

Common questions about this topic.

Q

What is Arrhythmogenic Right Ventricular Dysplasia 2 C1832931?

Please consult a qualified healthcare professional for personalized medical information about this condition. [Content pending medical review.]

general

Sources and references

Authoritative medical sources used to create this content.

1

Corrado D, Link MS, Calkins H. 2022 ESC Guidelines for the management of patients with ventricular arrhythmias and the prevention of sudden cardiac death. Eur Heart J. 2022;43(38):3889-3950.

guideline2022
2

Basso C, Corrado D, Marcus FI, Nava A, Thiene G. Arrhythmogenic right ventricular cardiomyopathy. Lancet. 2009;373(9671):1289-1300.

review2009
3

Philips B, te Riele AS, Sawant A, Calkins H, James CA. Outcomes in Patients with Arrhythmogenic Right Ventricular Cardiomyopathy Undergoing Ventricular Tachycardia Ablation. JACC Clin Electrophysiol. 2020;6(12):1519-1528.

clinical_trial2020
4

Baidya D, Bhattacharya P, Kumar MP, Singh P. Diagnostic Accuracy of Cardiac Magnetic Resonance Imaging in Arrhythmogenic Right Ventricular Cardiomyopathy: A Systematic Review and Meta-Analysis. Radiology. 2021;299(1):78-86.

meta_analysis2021

Medication Comparisons

Compare medications used to treat Arrhythmogenic Right Ventricular Dysplasia 2 C1832931. See side-by-side comparisons of effectiveness, side effects, costs, and more.

View Medication Comparisons

This information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.

Medical Disclaimer

This content is for general informational and educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. Always seek the guidance of a qualified healthcare provider with any questions you have about a medical condition, and never disregard professional medical advice or delay seeking it because of something you read here.

If you think you may have a medical emergency, call your local emergency number or go to the nearest emergency department immediately.

Medically reviewed by WellAlly Editorial Team Last reviewed August 25, 2026. · Read our editorial policy