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...

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Detalles Bibliográficos
Autores principales: Gomez, Andrew T., Prutkin, Jordan M., Rao, Ashwin L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2016
Materias:
Current Research
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

Internet

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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