Prenatal Diagnosis of Atrioventricular Block and QT Interval Prolongation by Fetal Magnetocardiography in a Fetus with Trisomy 18 and SCN5A R1193Q Variant
We report a case of fetal trisomy 18 with SCN5A R1193Q variant that presented with sinus bradycardia, 2 : 1 atrioventricular block (AVB), and QT interval prolongation. These complex arrhythmias were diagnosed by fetal magnetocardiography combined with ultrasound findings. Advanced AVB and ventricula...
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Published in | Case Reports in Pediatrics Vol. 2017; no. 2017; pp. 1 - 3 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
Cairo, Egypt
Hindawi Publishing Corporation
01.01.2017
Hindawi John Wiley & Sons, Inc Wiley |
Subjects | |
Online Access | Get full text |
ISSN | 2090-6803 2090-6811 |
DOI | 10.1155/2017/6570465 |
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Abstract | We report a case of fetal trisomy 18 with SCN5A R1193Q variant that presented with sinus bradycardia, 2 : 1 atrioventricular block (AVB), and QT interval prolongation. These complex arrhythmias were diagnosed by fetal magnetocardiography combined with ultrasound findings. Advanced AVB and ventricular arrhythmias were confirmed after birth. Genetic testing of the baby revealed a SCN5A R1193Q variant, which we considered could account for the various arrhythmias in this case. |
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AbstractList | We report a case of fetal trisomy 18 with SCN5A R1193Q variant that presented with sinus bradycardia, 2 : 1 atrioventricular block (AVB), and QT interval prolongation. These complex arrhythmias were diagnosed by fetal magnetocardiography combined with ultrasound findings. Advanced AVB and ventricular arrhythmias were confirmed after birth. Genetic testing of the baby revealed a SCN5A R1193Q variant, which we considered could account for the various arrhythmias in this case.We report a case of fetal trisomy 18 with SCN5A R1193Q variant that presented with sinus bradycardia, 2 : 1 atrioventricular block (AVB), and QT interval prolongation. These complex arrhythmias were diagnosed by fetal magnetocardiography combined with ultrasound findings. Advanced AVB and ventricular arrhythmias were confirmed after birth. Genetic testing of the baby revealed a SCN5A R1193Q variant, which we considered could account for the various arrhythmias in this case. We report a case of fetal trisomy 18 with R1193Q variant that presented with sinus bradycardia, 2 : 1 atrioventricular block (AVB), and QT interval prolongation. These complex arrhythmias were diagnosed by fetal magnetocardiography combined with ultrasound findings. Advanced AVB and ventricular arrhythmias were confirmed after birth. Genetic testing of the baby revealed a R1193Q variant, which we considered could account for the various arrhythmias in this case. We report a case of fetal trisomy 18 with SCN5A R1193Q variant that presented with sinus bradycardia, 2 : 1 atrioventricular block (AVB), and QT interval prolongation. These complex arrhythmias were diagnosed by fetal magnetocardiography combined with ultrasound findings. Advanced AVB and ventricular arrhythmias were confirmed after birth. Genetic testing of the baby revealed a SCN5A R1193Q variant, which we considered could account for the various arrhythmias in this case. We report a case of fetal trisomy 18 with SCN5A R1193Q variant that presented with sinus bradycardia, 2 : 1 atrioventricular block (AVB), and QT interval prolongation. These complex arrhythmias were diagnosed by fetal magnetocardiography combined with ultrasound findings. Advanced AVB and ventricular arrhythmias were confirmed after birth. Genetic testing of the baby revealed a SCN5A R1193Q variant, which we considered could account for the various arrhythmias in this case. |
Audience | Academic |
Author | Nozaki, Yoshihiro Takahashi-Igari, Miho Obata, Mana Lin, Lisheng Hamada, Hiromi Horigome, H. Kato, Yoshiaki |
AuthorAffiliation | 2 Department of Pediatric Cardiology, Ibaraki Children's Hospital, Mito, Japan 3 Department of Obstetrics and Gynecology, University of Tsukuba, Tsukuba, Japan 1 Department of Child Health, University of Tsukuba, Tsukuba, Japan |
AuthorAffiliation_xml | – name: 1 Department of Child Health, University of Tsukuba, Tsukuba, Japan – name: 2 Department of Pediatric Cardiology, Ibaraki Children's Hospital, Mito, Japan – name: 3 Department of Obstetrics and Gynecology, University of Tsukuba, Tsukuba, Japan |
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Cites_doi | 10.1136/jmg.2007.056333 10.1001/jama.2013.3219 10.1016/j.hrthm.2008.02.035 10.1046/j.1469-0705.2000.00292.x 10.1161/CIRCULATIONAHA.106.658021 10.1136/adc.2004.058115 10.1002/pd.2462 10.1111/j.1651-2227.2000.tb01189.x 10.1136/jmg.2003.013300 10.1016/j.hrthm.2013.04.020 |
ContentType | Journal Article |
Copyright | Copyright © 2017 Lisheng Lin et al. COPYRIGHT 2017 John Wiley & Sons, Inc. Copyright © 2017 Lisheng Lin et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Copyright © 2017 Lisheng Lin et al. 2017 |
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Snippet | We report a case of fetal trisomy 18 with SCN5A R1193Q variant that presented with sinus bradycardia, 2 : 1 atrioventricular block (AVB), and QT interval... We report a case of fetal trisomy 18 with SCN5A R1193Q variant that presented with sinus bradycardia, 2 : 1 atrioventricular block (AVB), and QT interval... We report a case of fetal trisomy 18 with R1193Q variant that presented with sinus bradycardia, 2 : 1 atrioventricular block (AVB), and QT interval... We report a case of fetal trisomy 18 with SCN5A R1193Q variant that presented with sinus bradycardia, 2: 1 atrioventricular block (AVB), and QT interval... We report a case of fetal trisomy 18 with SCN5A R1193Q variant that presented with sinus bradycardia, 2 : 1 atrioventricular block (AVB), and QT interval... |
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SubjectTerms | Arrhythmia Case Report Case studies Diagnosis Edwards' syndrome Heart block Methods Prenatal diagnosis |
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Title | Prenatal Diagnosis of Atrioventricular Block and QT Interval Prolongation by Fetal Magnetocardiography in a Fetus with Trisomy 18 and SCN5A R1193Q Variant |
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