A case of long QT syndrome having compound mutations of KCNH2 and SCN5A

Long QT syndrome (LQTS) is a hereditary ion channelopathy resulting in prolonged cardiac repolarization and abnormal prolongation of the QT interval on the electrocardiogram (ECG). The patients are likely to develop ventricular arrhythmias and sudden cardiac death. Molecular biology and basic electr...

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Vydáno v:J Cardiol Cases
Hlavní autoři: Ito, Saki, Taketani, Takeshi, Sugamori, Takashi, Okada, Taiji, Sato, Hirotomo, Adachi, Tomoko, Takeda, Masaki, Kodani, Nobuhiro, Takahashi, Nobuyuki, Endo, Akihiro, Yoshitomi, Hiroyuki, Tanabe, Kazuaki, Shimizu, Wataru
Médium: Artigo
Jazyk:Inglês
Vydáno: Japanese College of Cardiology 2012
Témata:
Case Report
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC6269416/
https://ncbi.nlm.nih.gov/pubmed/30533098
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jccase.2012.07.004
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