Congenital long QT syndrome: a case report of LQT2 and LQT13 in a neonate
R Bond, A Blaufox, B Goldner, A Patel - Europace, 2014 - academic.oup.com
Long QT syndrome (LQTS) is a disorder of ventricular myocardial repolarization
characterized by a prolonged QT interval on the electrocardiogram (ECG). At least 12 …
characterized by a prolonged QT interval on the electrocardiogram (ECG). At least 12 …
A novel KCNQ1 mutation in Chinese with congenital long QT syndrome
L Liang, ZD Du, LL Cai, JX Wu, T Zheng… - Zhonghua er ke za zhi …, 2003 - europepmc.org
Objective Congenital long QT syndrome (LQTS) is an inherited disorder of cardiac
repolarization characterized by prolongation of QT interval and polymorphic ventricular …
repolarization characterized by prolongation of QT interval and polymorphic ventricular …
Congenital Long QT Syndrome (LQTS) in Infancy: A Challenging Case
A Mohammed, M Rehab, H Moataz, Y Lemis - Cureus, 2024 - search.proquest.com
Long QT syndrome (LQTS), is an arrhythmia disorder, related to ventricular myocardial
repolarization characterized by a prolonged QT interval on the electrocardiogram that can …
repolarization characterized by a prolonged QT interval on the electrocardiogram that can …
[HTML][HTML] Congenital Long QT Syndrome (LQTS) in Infancy: A Challenging Case
M Aldirawi, R Musa, M Hamdi, L Yavuz - Cureus, 2024 - ncbi.nlm.nih.gov
Long QT syndrome (LQTS), is an arrhythmia disorder, related to ventricular myocardial
repolarization characterized by a prolonged QT interval on the electrocardiogram that can …
repolarization characterized by a prolonged QT interval on the electrocardiogram that can …
[PDF][PDF] Congenital long QT syndrome: a systematic review
E Galić, P Bešlić, P Kilić, Z Planinić, A Pašalić… - Acta Clinica …, 2021 - hrcak.srce.hr
Congenital long QT syndrome (LQTS) is a disorder of myocardial repolarization defined by a
prolonged QT interval on electrocardiogram (ECG) that can cause ventricular arrhythmias …
prolonged QT interval on electrocardiogram (ECG) that can cause ventricular arrhythmias …
Genomic structure of three long QT syndrome genes: KVLQT1, HERG, andKCNE1
I Splawski, J Shen, KW Timothy, GM Vincent… - Genomics, 1998 - Elsevier
Long QT syndrome (LQT) is a cardiac disorder causing syncope and sudden death from
arrhythmias. LQT is characterized by prolongation of the QT interval on electrocardiogram …
arrhythmias. LQT is characterized by prolongation of the QT interval on electrocardiogram …
A novel mutation of the KCNH2 gene in a family with congenital long QT syndrome
J Lian, J Zhou, X Huang, Y Wang… - … yi xue yi Chuan xue za …, 2010 - europepmc.org
Methods The medical record of the affected child and his parents were collected. The locus
of gene associated with the long QT syndrome was mapped by linkage analysis. Mutation …
of gene associated with the long QT syndrome was mapped by linkage analysis. Mutation …
Mutations at KCNQ1 and an unknown locus cause long QT syndrome in a large Australian family: Implications for genetic testing
KM Summers, NJ Bokil, FT Lu, JT Low… - American Journal of …, 2010 - Wiley Online Library
A large Australian family affected with long QT syndrome (LQTS) was studied. The medical
characteristics of the 16 clinically affected members were consistent with LQT1. A previously …
characteristics of the 16 clinically affected members were consistent with LQT1. A previously …
Long QT Syndrome: Presenting as Fetal Bradycardia
P Segaran, CN Kamalarathnam… - Journal of Clinical …, 2022 - journals.lww.com
Long QT syndromes (LQTSs) are inherited disorders of abnormal myocardial repolarization.
It is characterized by prolonged QT interval, T wave abnormalities, and tachyarrhythmias …
It is characterized by prolonged QT interval, T wave abnormalities, and tachyarrhythmias …
[PDF][PDF] Congenital long QT syndrome
BG Iskenderov, TV Lokhina, EA Molokova… - heart-vdj.com
Congenital long QT syndrome (LQTS) is the most common inherited arrhythmia in the
absence of structural heart disease [1–3]. LQTS is characterized by a genetically and …
absence of structural heart disease [1–3]. LQTS is characterized by a genetically and …