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==Overview==
==Overview==
==History and Symptoms==
===Symptoms===
Up to 80% of individuals with ARVD present with [[syncope]] or sudden cardiac death.  The remainder frequently present with palpitations or other symptoms due to right ventricular outflow tract (RVOT) tachycardia (a type of [[monomorphic ventricular tachycardia]]).
*[[Syncope]]:Up to 80% of individuals with ARVD present with [[syncope]] or sudden cardiac death.  The remainder frequently present with palpitations or other symptoms due to right ventricular outflow tract (RVOT) tachycardia (a type of [[monomorphic ventricular tachycardia]]).
 
Symptoms are usually exercise-related.  In populations where [[hypertrophic cardiomyopathy]] is screened out prior to involvement in competitive athletics, it is a common cause of sudden cardiac death.


Symptoms are usually exercise-related.
The first clinical signs of ARVD are usually during [[adolescence]].  However, signs of ARVD have been demonstrated in infants.
The first clinical signs of ARVD are usually during [[adolescence]].  However, signs of ARVD have been demonstrated in infants.



Revision as of 23:38, 22 September 2012

Arrhythmogenic right ventricular dysplasia Microchapters

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]

Overview

Symptoms

  • Syncope:Up to 80% of individuals with ARVD present with syncope or sudden cardiac death. The remainder frequently present with palpitations or other symptoms due to right ventricular outflow tract (RVOT) tachycardia (a type of monomorphic ventricular tachycardia).

Symptoms are usually exercise-related. The first clinical signs of ARVD are usually during adolescence. However, signs of ARVD have been demonstrated in infants.

Refernces

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