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Elusive Taussig–Bing anomaly/aortic valve atresia: a rare case of congenital heart disease—correlation of fetal and neonatal echo images and direct anatomical photographs

Elusive Taussig–Bing anomaly/aortic valve atresia: a rare case of congenital heart... Journal of Echocardiography (2020) 18:75–76 https://doi.org/10.1007/s12574-018-0414-4 C ASE IMAGE IN C ARDIO VASCUL AR ULTR ASOUND Elusive Taussig–Bing anomaly/aortic valve atresia: a rare case of congenital heart disease—correlation of fetal and neonatal echo images and direct anatomical photographs 1 1 Jonathan G. Dayan  · Brian C. Guenther Received: 9 October 2018 / Revised: 6 December 2018 / Accepted: 16 December 2018 / Published online: 1 January 2019 © Japanese Society of Echocardiography 2019 We present an extremely rare case of double outlet right ven- at the fetal, immediately post-natal, and intra-operative time tricle with malposed great arteries, sub-pulmonic ventricular periods for correlation and further appreciation of this detail- septal defect (Taussig–Bing anomaly) and aortic valve atre- oriented and technically demanding diagnostic process. This sia, of which there are no prior cases described. was a particularly dic ffi ult case to correctly diagnose in utero The mother was referred for fetal echocardiography sec- and highlights the challenges and limitations associated with ondary to concern for a cardiac anomaly on level 2 ana- fetal echocardiography, including the diminutive size of tomic obstetric ultrasound. Fetal echocardiogram performed certain fetal cardiac structures, maternal body habitus, fetal at 32 0/7 weeks gestation showed a large ventricular septal position and fetal movement. Due to these factors, http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Journal of Echocardiography Springer Journals

Elusive Taussig–Bing anomaly/aortic valve atresia: a rare case of congenital heart disease—correlation of fetal and neonatal echo images and direct anatomical photographs

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References (3)

Publisher
Springer Journals
Copyright
Copyright © Japanese Society of Echocardiography 2019
Subject
Medicine & Public Health; Cardiology; Ultrasound; Imaging / Radiology
ISSN
1349-0222
eISSN
1880-344X
DOI
10.1007/s12574-018-0414-4
Publisher site
See Article on Publisher Site

Abstract

Journal of Echocardiography (2020) 18:75–76 https://doi.org/10.1007/s12574-018-0414-4 C ASE IMAGE IN C ARDIO VASCUL AR ULTR ASOUND Elusive Taussig–Bing anomaly/aortic valve atresia: a rare case of congenital heart disease—correlation of fetal and neonatal echo images and direct anatomical photographs 1 1 Jonathan G. Dayan  · Brian C. Guenther Received: 9 October 2018 / Revised: 6 December 2018 / Accepted: 16 December 2018 / Published online: 1 January 2019 © Japanese Society of Echocardiography 2019 We present an extremely rare case of double outlet right ven- at the fetal, immediately post-natal, and intra-operative time tricle with malposed great arteries, sub-pulmonic ventricular periods for correlation and further appreciation of this detail- septal defect (Taussig–Bing anomaly) and aortic valve atre- oriented and technically demanding diagnostic process. This sia, of which there are no prior cases described. was a particularly dic ffi ult case to correctly diagnose in utero The mother was referred for fetal echocardiography sec- and highlights the challenges and limitations associated with ondary to concern for a cardiac anomaly on level 2 ana- fetal echocardiography, including the diminutive size of tomic obstetric ultrasound. Fetal echocardiogram performed certain fetal cardiac structures, maternal body habitus, fetal at 32 0/7 weeks gestation showed a large ventricular septal position and fetal movement. Due to these factors,

Journal

Journal of EchocardiographySpringer Journals

Published: Mar 1, 2020

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