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Studies of Magnesium in Congenital Long QT Syndrome
Pediatric Cardiology, 2002We studied the role of magnesium (Mg) in congenital long QT syndrome (LQTS). Twenty-two congenital LQTS patients and 30 control subjects were included in this study. We measured serum Mg (SMg) level and Mg retention (MgR) level, and evaluated the role of Mg (a high MgR level reflects Mg deficiency in the body).
K, Hoshino +3 more
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Anesthesia eJournal
Context: Congenital long QT syndrome (cLQTS) is the most common genetic cardiac ion channelopathy in the US. Patients with cLQTS are at risk for ventricular tachycardia (VT) in the “torsades de pointes” (TdP) pattern from physical and emotional stress, including during the perioperative period.
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Context: Congenital long QT syndrome (cLQTS) is the most common genetic cardiac ion channelopathy in the US. Patients with cLQTS are at risk for ventricular tachycardia (VT) in the “torsades de pointes” (TdP) pattern from physical and emotional stress, including during the perioperative period.
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Genetics of Congenital Long Qt Syndrome and Brugada Syndrome
Future Cardiology, 2008The inherited cardiac arrhythmias including congenital and acquired long QT syndrome (LQTS), Brugada syndrome, progressive cardiac conduction defect, catecholaminergic polymorphic ventricular tachycardia, arrhythmogenic right ventricular cardiomyopathy, familial atrial fibrillation, familial sick sinus syndrome and short QT syndrome, are linked to ...
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[Congenital long QT syndrome].
Archives de pediatrie : organe officiel de la Societe francaise de pediatrie, 2001Long QT syndrome (LQTS) is a clinically and genetically heterogenous syndrome characterized by a lengthening of the QT interval on the surface ECG and a propensity to severe ventricular arrhythmias such as torsades de pointes and ventricular fibrillation, leading eventually to syncope and sudden death.
J M, Lupoglazoff +4 more
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[Congenital long QT syndrome].
Presse medicale (Paris, France : 1983), 1998SEVERAL FORMS: Congenital long QT syndrome is a clinically (with and without deafness) and genetically (recessive or dominant autosomal inheritance) heterogeneous entity characterized by a long QT interval on the ECG associated with the risk of severe ventricular arrhythmia (torsade de pointes, ventricular fibrillation) and subsequent syncope or sudden
Lupoglazoff, J +5 more
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Precision therapy in congenital long QT syndrome
Trends in Cardiovascular MedicineLong QT syndrome (LQTS) is a potentially life-threatening, but highly treatable genetic heart disease. LQTS-directed therapies often consist of beta-blockers (BBs), left cardiac sympathetic denervation (LCSD), and/or an implantable cardioverter defibrillator (ICD).
Raquel, Neves +5 more
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Congenital long QT and short QT syndromes
2009The most recent findings of Long and Short QT Syndrome are ...
Schwartz, PJ, Crotti, L
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An Overview of Congenital Long QT Syndrome
The Journal of Continuing Education in Nursing, 2005openaire +2 more sources