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See Latest ArticlesCongenital long QT syndrome
BMC Cardiovascular Disorders, 07/08/08
Crotti L et al. - 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. The prognosis of the disease is usually good in patients that are correctly diagnosed and treated. However, there are a few exceptions: patients with Timothy syndrome, patients with Jervell Lange-Nielsen syndrome carrying KCNQ1 mutations and LQT3 patients with 2:1 atrio-ventricular block and very early occurrence of cardiac arrhythmias.
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Today in Cardiovascular...keeping you current
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Relation of Nausea and Vomiting in Acute Myocardial Infarction to Location of the Infarct
The American Journal of Cardiology, 12/15/09
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Scandinavian Journal of Trauma, Resuscitation and Emergency Medicine, 12/15/09
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