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An Adolescent with Possible Arrhythmogenic Right Ventricular Dysplasia and Long QT Syndrome: Evaluation and Management

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...

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Detalles Bibliográficos
Publicado en:Ann Noninvasive Electrocardiol
Main Authors: Tisma‐Dupanovic, Svjetlana, Wagner, Jonathan B., Shah, Sanket, Huang, David T., Moss, Arthur J.
Formato: Artigo
Idioma:Inglês
Publicado: John Wiley and Sons Inc. 2013
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Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC6932431/
https://ncbi.nlm.nih.gov/pubmed/23347029
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1111/anec.12043
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