Background: Long QT syndrome (LQTS) is a disorder in which electrical cardiac ventricular repolarization is impaired. It results in an increased risk of an irregular heartbeat which can result in palpitations, fainting, drowning, or sudden death. Long QT Syndrome may present as tonic-clonic seizure or a seizure-like disorder. By taking a superficial electrocardiogram (ECG) and proper diagnosis,...

background:cardiovascular effects of acute organophosphate (op) poisoning are common. this study was aimed to assess the cardiovascular effects of op poisoned patients in nepal. methods:this was a prospective hospital-based cross-sectional study of 115 acute op poisoned patients presenting in emergency department of a tertiary care teaching hospital of central nepal during november 2008 to octo...

torsades de pointes is a rare but potentially lethal arrhythmia which mainly occurs in the setting of a prolonged qt interval. ecg is a reliable tool to detect such abnormalities, routinely taken from all patients over 40 who undergo surgery. we describe the case of a 35-year-old woman with torsades de points arrhythmia after hysterectomy surgery. most likely, our patients had long qt syndrome ...

Torsades de pointes is a rare but potentially lethal arrhythmia which mainly occurs in the setting of a prolonged QT interval. ECG is a reliable tool to detect such abnormalities, routinely taken from all patients over 40 who undergo surgery. We describe the case of a 35-year-old woman with torsades de points arrhythmia after hysterectomy surgery. Most likely, our patients had long QT syndro...

torsades de pointes is a rare but potentially lethal arrhythmia which mainly occurs in the setting of a prolonged qt interval. ecg is a reliable tool to detect such abnormalities, routinely taken from all patients over 40 who undergo surgery. we describe the case of a 35-year-old woman with torsades de points arrhythmia after hysterectomy surgery. most likely, our patients had long qt syndrome ...

introduction: congenital long qt syndrome (lqts) is a cardiac disorder characterized by qt interval prolongation at basal ecg. different lqts genes encode ion channel subunits or proteins involved in regulating cardiac ionic currents. long qt syndrome type 6 (lqt6) is caused by mutation in the kcne2 gene. our research aimed to analyze genetic variants of kcne2 gene causing the disease in irania...

objective(s): as mitochondrial oxidative stress is probably entailed in atp production, a candidate modifier factor for the long qt syndrome (lqts) could be mitochondrial dna (mtdna). it has been notified that ion channels' activities in cardiomyocytes are sensitive to the atp level. materials and methods: the sample of the research was an iranian family with lqts for mutations by pcr-sscp...

genetic basis of diffrent arrhythmias has always been an intresting subject of resesrch for scientists. here i will review in brief the most common familia arrhythmias and the new findings regarding their mode of inhetitance. this paper will mainly focus on the genetic basis of the long qt syndromes but we will also have a short review of the genetics of three other familia congenital arrhythmo...