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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Zapisane w:
Opis bibliograficzny
Wydane w:Ann Noninvasive Electrocardiol
Główni autorzy: Tisma‐Dupanovic, Svjetlana, Wagner, Jonathan B., Shah, Sanket, Huang, David T., Moss, Arthur J.
Format: Artigo
Język:Inglês
Wydane: John Wiley and Sons Inc. 2013
Hasła przedmiotowe:
Hereditary Arrhythmia Corner: Learning from Challenging Patients
Dostęp online: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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