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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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Vydáno v:Ann Noninvasive Electrocardiol
Hlavní autoři: Tisma‐Dupanovic, Svjetlana, Wagner, Jonathan B., Shah, Sanket, Huang, David T., Moss, Arthur J.
Médium: Artigo
Jazyk:Inglês
Vydáno: John Wiley and Sons Inc. 2013
Témata:
On-line přístup: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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