Congenital long QT syndrome: A case report

The congenital long QT syndrome (LQTS) is characterized by abnormally prolonged ventricular repolarization due to inherited defects in cardiac sodium and potassium channels, which predispose the patients to syncope, seizure like activity, ventricular arrhythmias, and sudden cardiac death. Early diag...

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Detalles Bibliográficos
Main Authors: Aziz, Fahad, Penupolu, Sudheer, Doddi, Sujatha, Togonu-Bickersteth, Babajide, Ameen, Abdul
Formato: Artigo
Idioma:Inglês
Publicado: Pioneer Bioscience Publishing Company 2010
Assuntos:
Case Report
Acceso en liña:https://ncbi.nlm.nih.gov/pmc/articles/PMC3256463/
https://ncbi.nlm.nih.gov/pubmed/22263042
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3978/j.issn.2072-1439.2010.02.03.12
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