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Congenital Long QT Syndrome Type 8 Characterized by Fetal Onset of Bradycardia and 2:1 Atrioventricular Block |
Donghoon Joo, Hyoung Doo Lee, Taehong Kim, Hoon Ko, Joung-Hee Byun |
Neonatal Med. 2021;28(1):59-63. Published online February 24, 2021 DOI: https://doi.org/10.5385/nm.2021.28.1.59 |
Congenital Long QT Syndrome Type 8 Characterized by Fetal Onset of Bradycardia and 2:1 Atrioventricular Block Congenital long QT syndrome inducing 2:1 atrioventricular block: early detection in fetal life Congenital Long QT Syndrome Type 2 with Symptomatic 2:1 Atrioventricular Block and Ventricular Arrhythmia in a Preterm Baby Who Presented with Fetal Ventricular Tachycardia and Hydrops Sustained fetal bradycardia with 1:1 atrioventricular conduction and long QT syndrome Congenital Long QT Syndrome and 2:1 Atrioventricular Block with a Mutation of the SCN5A Gene Two:One atrioventricular block in infants with congenital long QT syndrome T-Wave Alternans, QRST-Wave Alternans and Atrioventricular Block: Three Consecutive Rate-Dependent Phenomena in a Child with Congenital Long-QT Syndrome Fetal Atrioventricular Block and Postpartum Augmentative QT Prolongation in a Patient With Long-QT Syndrome With KCNQ1 Mutation Successful prenatal management of ventricular tachycardia and second-degree atrioventricular block in fetal long QT syndrome Infants with long-QT syndrome and 2:1 atrioventricular block |