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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Detalhes bibliográficos
Publicado no:Ann Noninvasive Electrocardiol
Main Authors: Tisma‐Dupanovic, Svjetlana, Wagner, Jonathan B., Shah, Sanket, Huang, David T., Moss, Arthur J.
Formato: Artigo
Idioma:Inglês
Publicado em: John Wiley and Sons Inc. 2013
Assuntos:
Hereditary Arrhythmia Corner: Learning from Challenging Patients
Acesso em linha: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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