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- W2038194364 abstract "Long QT syndrome (LQTS) is an uncommon genetic disease that affects approximately 1 in 2500 people and can present with syncope, cardiogenic seizures, and/or sudden cardiac death. This cardiac channelopathy stems from delayed cardiac repolarization that is characterized by a prolonged QT interval on a 12-lead electrocardiogram (ECG). 1 Moss A.J. Long QT syndrome. JAMA. 2003; 289: 2041-2044 Crossref PubMed Scopus (222) Google Scholar The patient's LQTS substrate can deteriorate into its trademark arrhythmia of torsades de pointes." @default.
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- W2038194364 date "2012-02-01" @default.
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- W2038194364 title "Congenital type 1 long QT syndrome unmasked by a highly caffeinated energy drink" @default.
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- W2038194364 doi "https://doi.org/10.1016/j.hrthm.2011.10.011" @default.
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