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Evaluation and Management of Athletes With Long QT Syndrome: An Evolved Paradigm
CONTEXT: The congenital long QT syndrome (LQTS) is an inherited channelopathy known for its electrocardiographic manifestations of QT prolongation and its hallmark arrhythmia, torsades de pointes (TdP). TdP can lead to syncope or sudden death and is often precipitated by triggers such as physical ex...
Autores principales: | Gomez, Andrew T., Prutkin, Jordan M., Rao, Ashwin L. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5089354/ https://www.ncbi.nlm.nih.gov/pubmed/27480102 http://dx.doi.org/10.1177/1941738116660294 |
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