Results 11 to 20 of about 7,883,789 (150)
GENETIC ASPECTS OF CONGENITAL LONG QT SYNDROME [PDF]
Рациональная фармакотерапия в кардиологии, 2015 The main symptoms and clinical types of long QT syndrome are described. Molecular genetic diagnostics and updated approaches to the management of patients with long QT syndrome arepresented.
A. A. Chernova +2 more
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Sudden Cardiac Arrest in the Postpartum Period Due to Long QT Syndrome and Dilated Cardiomyopathy
JACC: Case Reports, 2023 We describe the case of a previously healthy patient presenting with sudden cardiac arrest in the postpartum period as a result of concomitant congenital type 1 long QT syndrome and BAG3 dilated cardiomyopathy.
Daniel R. Patterson, MD +3 more
doaj +2 more sources
The congenital long QT syndrome Type 3: An update
Indian Pacing and Electrophysiology Journal, 2018 Congenital long QT syndrome type 3 (LQT3) is the third in frequency compared to the 15 forms known currently of congenital long QT syndrome (LQTS). Cardiac events are less frequent in LQT3 when compared with LQT1 and LQT2, but more likely to be lethal ...
Andrés Ricardo Pérez-Riera +5 more
doaj +2 more sources
Comparative Characteristics of Beta-Blockers in Patients with Congenital Long QT Syndrome [PDF]
Рациональная фармакотерапия в кардиологии, 2021 Congenital long QT syndrome is a pathology that requires special attention and knowledge about the safety and effectiveness of various medications.
A. Yu. Proshlyakov +2 more
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Congenital long QT syndrome [PDF]
Orphanet Journal of Rare Diseases, 2008 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. Disease prevalence is estimated at close to 1 in 2,500 live births. The
Celano Giuseppe +3 more
doaj +2 more sources
Hyperpyrexia associated with congenital Long QT Syndrome [PDF]
Çukurova Üniversitesi Tıp Fakültesi Dergisi, 2014 Congenital long QT syndrome (CLQTS) is a genetic disorder presented with prolonged QT interval. In these patients, risk of sudden cardiac death due to ventricular tachyarrhythmias is high.
Nuriye Tarakci +4 more
doaj +3 more sources
Long QT syndrome - causes and risk factors [PDF]
Journal of Education, Health and Sport, 2018 Sudden cardiac death is a major public health challenge, which can be caused by genetic or acquired structural or electrophysiological abnormalities. These abnormalities include channelopathies such as long QT, short QT and Brugada syndromes.
Erwin Ciechański +3 more
doaj +4 more sources
A Congenital Deadly Association: Dilated Cardiomyopathy and Long QT Syndrome [PDF]
Journal of Cardiac Arrhythmias, 2020 Long QT syndrome is one of the most feared entities in hospitalized patients due to the potential risk for ventricular tachycardia and sudden death. Association between channelopathies and congenital cardiomyopathy is a new entity that has been studied ...
Neiberg de Alcantara Lima +3 more
doaj +7 more sources
T-wave alternans in long QT syndrome
Annals of Pediatric Cardiology, 2018 Long QT syndrome (LQTS) is a congenital disorder characterized by prolongation of QT interval in the electrocardiogram (ECG) and a propensity to develop ventricular arrhythmias, which may lead to syncope, cardiac arrest or sudden death. T-wave alternans (
Siddharth Narayan Gadage
doaj +2 more sources
Journal of Arrhythmia, 2017 A 7-year-old boy presented at our hospital with syncope. At birth, electrocardiography had shown a long QT interval with torsade de pointes (TdP). Congenital long QT syndrome (LQTS) had been diagnosed by genetic testing, and was successfully controlled ...
Hirotaro Sugiyama, MD +9 more
doaj +2 more sources