Understanding Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC)

Friday, 13 September 2024, 08:00

Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC) is a genetic condition affecting the heart muscle. This disorder can lead to arrhythmias, heart failure, and sudden cardiac death among affected individuals. Early diagnosis and management of ARVC are crucial for improving outcomes and quality of life.
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Understanding Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC)

Overview of Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC)

Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC) is primarily a genetic disorder that impacts the heart's structure, specifically the right ventricle. Patients may experience varied symptoms, including severe cardiac arrhythmias that can ultimately lead to significant health complications.

Symptoms and Diagnosis

  • Symptoms often include palpitations and dizziness.
  • Diagnosis typically involves echocardiograms and genetic testing.

Treatment Options for ARVC

Management strategies for ARVC focus on preventing sudden cardiac death and may comprise lifestyle adjustments, medication, or surgical interventions:

  1. Medications to control heart rate and rhythm.
  2. Implantable cardioverter-defibrillators (ICDs) for high-risk patients.
  3. Regular cardiology follow-ups for monitoring progress.

This article was prepared using information from open sources in accordance with the principles of Ethical Policy. The editorial team is not responsible for absolute accuracy, as it relies on data from the sources referenced.


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