Results 31 to 40 of about 38,746 (286)
Sex differences in long QT syndrome
Frontiers in Cardiovascular Medicine, 2023 Long QT Syndrome (LQTS) is a rare, inherited channelopathy characterized by cardiac repolarization dysfunction, leading to a prolonged rate-corrected QT interval in patients who are at risk for malignant ventricular tachyarrhythmias, syncope, and even ...
Nuria Díez-Escuté +18 more
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Resuscitation of sudden cardiac death caused by acute epileptic seizures: A case report
Journal of Acute Disease, 2016 Symptomatic long QT syndrome in pediatric patients is a life-threatening condition. Sometimes, this pathology can be misdiagnosed and erroneously managed as generalized epilepsy due to similar clinical manifestations.
Dana-Oliviana Geavlete +7 more
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Long QT syndrome – Bench to bedside
Heart Rhythm O2, 2021 Long QT syndrome (LQTS) is a cardiovascular disorder characterized by an abnormality in cardiac repolarization leading to a prolonged QT interval and T-wave irregularities on the surface electrocardiogram. It is commonly associated with syncope, seizures,
Daniela Ponce-Balbuena, PhD +1 more
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Long QT in stunned myocardium: unrecognised cause of acquired long QT syndrome
Journal of Medical Science, 2014 Long QT syndrome (LQTS) is a heart disorder characterized by a prolongation of the QT interval on ECG and a predisposition to ventricular tachyarrhythmias, which may lead to syncope, cardiac arrest or sudden cardiac death. This condition may be inherited
Jerzy Sacha
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Congenital long QT syndrome in children [PDF]
Medicinski Podmladak, 2016 Long QT syndrome (LQTS) is a cardiac repolarization disorder characterized by prolonged QT interval on the electrocardiogram (ECG) and increased propensity to ventricular tachyarrhythmias and cardiac events.
Cerović Ivana, Košutić Jovan
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Prevalence of Long QT Syndrome in Children with Congenital Sensory-Neural Deafness
Journal of Ardabil University of Medical Sciences, 2021 Background & objectives: Long QT syndrome (LQTS), congenital or acquired disorder, is characterized by a prolonged QT interval associated with syncope attacks and sudden death.
Ahmad Jamei Khosroshahi +4 more
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Comparative Characteristics of Beta-Blockers in Patients with Congenital Long QT Syndrome
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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Late-onset severe long QT syndrome.
, 2017 We report a case of torsades de pointes arrhythmia as the first manifestation of congenital Long QT syndrome in a 77-year-old man with family history of sudden unexplained death.
Schaller, André +7 more
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QT Adaptation and Intrinsic QT Variability in Congenital Long QT Syndrome
Journal of the American Heart Association: Cardiovascular and Cerebrovascular Disease, 2015 Background Increased variability of QT interval (QTV) has been linked to arrhythmias in animal experiments and multiple clinical situations. Congenital long QT syndrome (LQTS), a pure repolarization disease, may provide important information on the ...
Srikanth Seethala +5 more
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Long QT syndrome and anaesthesia [PDF]
British Journal of Anaesthesia, 2003 Long QT syndrome (LQTS) is an arrhythmogenic cardiovascular disorder resulting from mutations in cardiac ion channels. LQTS is characterized by prolonged ventricular repolarization and frequently manifests itself as QT interval prolongation on the electrocardiogram (ECG). The age at presentation varies from in utero to adulthood.
P D, Booker, S D, Whyte, E J, Ladusans
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