Long QT syndrome (LQTS) is a potentially life-threatening cardiac repolarization disorder characterized by an increased risk of fatal arrhythmias. Accurate and timely diagnosis is …
B Takase, T Ikeda, W Shimizu, H Abe, T Aiba… - Circulation …, 2024 - jstage.jst.go.jp
Sinus node dysfunction may be either transient (reversible/physiological) due to the involvement of the autonomic nervous system or pharmaceuticals, or chronic due to …
Aims Congenital long-QT syndromes (cLQTS) or drug-induced long-QT syndromes (diLQTS) can cause torsade de pointes (TdP), a life-threatening ventricular arrhythmia. The current …
G Tse, S Lee, J Zhou, T Liu, ICK Wong… - Frontiers in …, 2021 - pmc.ncbi.nlm.nih.gov
Introduction: Congenital long QT syndrome (LQTS) is a cardiac ion channelopathy that predisposes affected individuals to spontaneous ventricular tachycardia/fibrillation (VT/VF) …
Abstract Background Long QT syndrome (LQTS) predisposes individuals to arrhythmic syncope or seizure, sudden cardiac arrest, or sudden cardiac death (SCD). Increased …
BJM Hermans, FC Bennis, AS Vink, T Koopsen, A Lyon… - Heart Rhythm, 2020 - Elsevier
Background Diagnosing long QT syndrome (LQTS) remains challenging because of a considerable overlap in QT interval between patients with LQTS and healthy subjects …
N Niimi, K Yuki, K Zaleski - Journal of Cardiothoracic and Vascular …, 2022 - jcvaonline.com
TORSADES DE pointes (TdP or “twisting of the points”) is a rare but potentially fatal polymorphic ventricular tachycardia characterized by rapid, wide QRS complexes of …
Background Pathogenic/likely pathogenic (P/LP) variants in the KCNQ1-encoded Kv7. 1 potassium channel cause type 1 long QT syndrome (LQT1). Despite the revamped 2015 …
Abstract Long QT syndrome (LQTS), Brugada syndrome (BrS), and catecholaminergic polymorphic ventricular tachycardia (CPVT) are genetic diseases of the heart caused by …