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Details
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Written by Mohammed Haroon Rashid, Kakhaber Etsadashvilli, Anzor Melia, Khatuna Jalabadze, and Ia Avaliani
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Parent Category: Browse issues of Electronic Physician by year and volume
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Category: Year 2010, Volume 2
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Hits: 94051
Abstract
Long QT syndrome (LQTS) is an inherited ion channelopathy resulting in abnormal ventricular repolarization and abnormal prolongation of QT interval on the ECG. Syncope, fainting, cardiac arrest, and sudden death are common manifestations of LQTS. We present a case report that describes a patient with prolonged QT interval after extrasystoles and a family history of sudden cardiac deaths.
Key words: Long QT syndrome; Sudden cardiac death; Extrasystoles
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