اقبالی, علیاشرف ,
اکبری اسبق, ناصرالدین ,
اکبری اسبق, پروین ,
کیهانیدوست, زرینتاج ,
Background: Long QT syndromes (LQT) are genetic abnormalities of ventricular repo-larization, with an estimated incidence of about one per 10000 births. It is characterized by prolongation of the QT interval in electrocardiogram (EKG) and associated with a high risk for syncope and sudden death in patients. Type of this syndrome is association with congenital deafness. Our objective was to eval...
