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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Veröffentlicht in:J Cardiol Cases
Hauptverfasser: 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
Format: Artigo
Sprache:Inglês
Veröffentlicht: Japanese College of Cardiology 2012
Schlagworte:
Case Report
Online Zugang: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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