• J Electrocardiol · Sep 2015

    Review Case Reports

    Arrythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) and cathecholaminergic polymorphic ventricular tachycardia (CPVT): A phenotypic spectrum seen in same patient.

    • Hiten Patel, Priyank Shah, Upamanyu Rampal, Fayez Shamoon, and Satish Tiyyagura.
    • Division of Cardiology, Department of Medicine, Saint Michael's Medical Center, New York Medical College, Newark, NJ, United States. Electronic address: hiten0409@yahoo.com.
    • J Electrocardiol. 2015 Sep 1; 48 (5): 874-8.

    AbstractARVD/C and CPVT are rare inheritable sudden cardiac death syndromes predominantly expressed in younger individuals. ARVD/C is characterized by a progressive fibrofatty replacement of the myocardium that predisposes to ventricular tachycardia while CPVT is characterized by exercise induced bidirectional/polymorphic ventricular tachycardia (VT) and a structurally normal heart. A mutation in different genes causes these syndromes but recently, mutation in a common gene RYR2 has been associated with both disorders and it has been suggested that CPVT and ARVD/C represent a phenotypic spectrum. We present a case unique in expressing both these phenotypes. Copyright © 2015. Published by Elsevier Inc.

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