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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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Bibliografski detalji
Izdano u:Ann Noninvasive Electrocardiol
Glavni autori: Tisma‐Dupanovic, Svjetlana, Wagner, Jonathan B., Shah, Sanket, Huang, David T., Moss, Arthur J.
Format: Artigo
Jezik:Inglês
Izdano: John Wiley and Sons Inc. 2013
Teme:
Online pristup: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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