Long QT syndromeTriple mutationKCNH2 geneKCNQ1 geneSCN5A genePolymorphic ventricular tachycardiaCongenital long QT syndrome (LQTS) is a rare hereditary disease, with an incidence of 1 in 2000, characterized by prolonged ventricular repolarization and malignant ventricular tachyarrhythmias. We report the ...
网络综合征;间期延长综合征;延长综合症 网络释义 1. 综合征 长QT综合征(long QT syndrome)合并先天性耳聋,又名聋- 心综合征(surdo-cardiac syndrome),为常染色体隐性遗传病,有心 … zhidao.baidu.com|基于4个网页 2. 间期延长综合征 QT延长... ... ) Long QT syndrome 延长综合征 )long QT syndrome间期...
Long QT syndrome (LQTS) is characterized by prolongation of the QT interval on the surface electrocardiogram (EKG) that can result in symptomatic ventricular arrhythmias. The symptoms can include palpitations, syncope, and sudden cardiac arrest. The prolonged QT interval reflects abnormal ventricular rep...
In this article, author Dr. Kathy Glatter discusses the use of genetic testing for finding cardiac syndromes such as long QT syndrome. Case History A 34-year-old female with long QT syndrome (LQTS) was referred to our institution for evaluation. Starting
Long-QT syndrome (LQT, LQTS, Romano-Ward syndrome, subgroups: Jervell & Lange-Nielsen syndrome, Andersen-Tawil syndrome, Timothy syndrome, Ankyrin-B syndrome, Cardiac-only Timothy syndrome, Triadin knockout syndrome). Comment: It may be appropriate to limit the use of numbered LQTS to LQTS 1...
Long QT syndrome & torsade de pointes 长QT综合征,尖端扭转型室性心动过速 从题目可以看出长QT嘛,就是QT延长了呗,这后面看着不像英文的,猜下是什么语言←_← 法语嘛(昂首挺胸) 英文的翻译叫做twisting of the points,中文大家都能看的懂,说白点尖端尖端就是QRS主波的方向一直在换=。=我还记得我们诊断书上...
Congenital long QT syndrome (LQTS) is a hereditary cardiac disease characterized by a prolongation of the QT interval at basal ECG and by a high risk of life-threatening arrhythmias. Disease prevalence is estimated at close to 1 in 2,500 live births. The two cardinal manifestations of LQTS ...
It is becoming clear that mutations in the KVLQT1, human "ether-a-go-go" related gene, cardiac voltage-dependent sodium channel gene, minK and MiRP1 genes, respectively, are responsible for the LQT1, LQT2, LQT3, LQT5 and LQT6 variants of the Romano-Ward syndrome, characterized by auto...
The hereditary long QT syndrome (LQTS) is a genetic channelopathy with variable penetrance that is associated with increased propensity to syncope, polymorphous ventricular tachycardia (torsades de pointes), and sudden arrhythmic death. This inherited cardiac disorder constitutes an important cause of mali...
Congenital long QT syndrome (LQTS) is a rare hereditary disease, with an incidence of 1 in 2000, characterized by prolonged ventricular repolarization and malignant ventricular tachyarrhythmias. We report the case of a 30-year-old woman, previously diagnosed with neurocardiogenic syncope, in whom LQ...