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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Bibliografische gegevens
Gepubliceerd in:J Arrhythm
Hoofdauteurs: Sugiyama, Hirotaro, Tachibana, Motomi, Morita, Hiroshi, Nishii, Nobuhiro, Miyoshi, Akihito, Sugiyama, Hiroyasu, Nakagawa, Koji, Watanabe, Atsuyuki, Nakamura, Kazufumi, Ito, Hiroshi
Formaat: Artigo
Taal:Inglês
Gepubliceerd in: Elsevier 2017
Onderwerpen:
Case Report
Online toegang: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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