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...

Deskribapen osoa

Gorde:
Xehetasun bibliografikoak
Argitaratua izan da:J Arrhythm
Egile Nagusiak: Sugiyama, Hirotaro, Tachibana, Motomi, Morita, Hiroshi, Nishii, Nobuhiro, Miyoshi, Akihito, Sugiyama, Hiroyasu, Nakagawa, Koji, Watanabe, Atsuyuki, Nakamura, Kazufumi, Ito, Hiroshi
Formatua: Artigo
Hizkuntza:Inglês
Argitaratua: Elsevier 2017
Gaiak:
Case Report
Sarrera elektronikoa: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
Etiketak: Etiketa erantsi
Etiketarik gabe, Izan zaitez lehena erregistro honi etiketa jartzen!

Antzeko izenburuak