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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Detalhes bibliográficos
Publicado no:J Arrhythm
Main Authors: Sugiyama, Hirotaro, Tachibana, Motomi, Morita, Hiroshi, Nishii, Nobuhiro, Miyoshi, Akihito, Sugiyama, Hiroyasu, Nakagawa, Koji, Watanabe, Atsuyuki, Nakamura, Kazufumi, Ito, Hiroshi
Formato: Artigo
Idioma:Inglês
Publicado em: Elsevier 2017
Assuntos:
Case Report
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5459415/
https://ncbi.nlm.nih.gov/pubmed/28607621
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.joa.2016.10.561
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