Seminars in Pediatric Neurology
Volume 12, Issue 1 , Pages 25-31, March 2005

Hypertrophic Cardiomyopathy and Arrhythmogenic Right Ventricular Dysplasia in Young Patients

  • Patricio A. Frias, MD

      Affiliations

    • Corresponding Author InformationAddress reprint requests to Patrick A. Frias, MD, Sibley Heart Center Cardiology, 52 Executive Park South, Suite 5200, Atlanta, Georgia 30329.

Sibley Heart Center Cardiology, Children’s Healthcare of Atlanta, Emory University School of Medicine, Atlanta, GA.

The annual incidence of sudden cardiac death in young athletes is approximately 1 in 200,000. The most common causes include hypertrophic cardiomyopathy and arrhythmogenic right ventricular dysplasia/cardiomyopathy. These genetic disorders typically manifest in the second decade of life and have the potential for sudden death as the first symptom. Medical care providers must be aware of these disease entities when evaluating patients with seizures, syncope, and/or palpitations. The purpose of this article is to describe their genetics, clinical presentation, and diagnosis.

To access this article, please choose from the options below

Login to an existing account or Register a new account.

  • Purchase this article for 10.00 USD (You must login/register to purchase this article)

    Online access for 24 hours. The PDF version can be downloaded as your permanent record.

  • Subscribe to this title

    Get unlimited online access to this article and all other articles in this title 24/7 for one year.

  • Claim access now

    For current subscribers with Society Membership or Account Number.

  • Visit SciVerse ScienceDirect to see if you have access via your institution.
 

PII: S1071-9091(04)00103-2

doi:10.1016/j.spen.2004.11.003

Seminars in Pediatric Neurology
Volume 12, Issue 1 , Pages 25-31, March 2005