医学
动脉导管
完全性肺静脉畸形连接
心室
肺动脉闭锁
低出生体重
内科学
心脏病学
怀孕
遗传学
生物
作者
Yasuhiro Inoue,Hiroyuki Suzuki,Shingo Kasahara,Yasuhiro Kotani
标识
DOI:10.1016/j.jtcvs.2023.07.040
摘要
The present investigation was approved by the institutional review board of the authors’ hospital. Given the observational nature of the study, requirements for informed written consent were waived (IRB-2009-023; approval, October 23, 2020). A 10-day-old girl weighing 1998 g at birth with right atrial isomerism, functional single ventricle, pulmonary atresia, bilateral superior venous cava, patent ductus arteriosus (PDA), right aortic arch, infracardiac total anomalous pulmonary venous connection (TAPVC), and patent ductus venosus (DV) underwent a Fontan repair procedure after several palliations (Figures 1 and 2).
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