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We describe a unique presentation of arrhythmogenic right ventricular dysplasia (ARVD) in a 14-year-old Caucasian male who was additionally diagnosed with long QT syndrome (LQTS). Genetic testing eventually confirmed the diagnosis of both ARVD and LQTS, which combined, to our knowledge, has not been reported in the literature. ©2013, Wiley Periodicals, Inc.

Citation

Svjetlana Tisma-Dupanovic, Jonathan B Wagner, Sanket Shah, David T Huang, Arthur J Moss. An adolescent with possible arrhythmogenic right ventricular dysplasia and long QT syndrome: evaluation and management. Annals of noninvasive electrocardiology : the official journal of the International Society for Holter and Noninvasive Electrocardiology, Inc. 2013 Jan;18(1):75-8

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PMID: 23347029

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