Epicardially placed implantable cardioverter-defibrillator for a child with congenital long QT syndrome

A 7-year-old boy presented at our hospital with syncope. At birth, electrocardiography had shown a long QT interval with torsade de pointes (TdP). Congenital long QT syndrome (LQTS) had been diagnosed by genetic testing, and was successfully controlled with oral propranolol. At age 7, TdP had recurr...

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Detalles Bibliográficos
Autores principales: Sugiyama, Hirotaro, Tachibana, Motomi, Morita, Hiroshi, Nishii, Nobuhiro, Miyoshi, Akihito, Sugiyama, Hiroyasu, Nakagawa, Koji, Watanabe, Atsuyuki, Nakamura, Kazufumi, Ito, Hiroshi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2017
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5459415/
https://www.ncbi.nlm.nih.gov/pubmed/28607621
http://dx.doi.org/10.1016/j.joa.2016.10.561

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5459415/
https://www.ncbi.nlm.nih.gov/pubmed/28607621
http://dx.doi.org/10.1016/j.joa.2016.10.561

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