主动脉闭锁合并单心室且心室情况不明。
Aortic atresia with a solitary and indeterminate ventricle.
作者信息
Darwish A, Higa T, Collins-Nakai R L
机构信息
Department of Pediatrics, University of Alberta, Edmonton, Canada.
出版信息
Int J Cardiol. 1988 Jan;18(1):97-101. doi: 10.1016/0167-5273(88)90035-6.
PMID:3343068
Abstract
A male infant having aortic atresia and double inlet to a solitary and indeterminate ventricle, presented a clinical picture of "hypoplastic left heart syndrome". Haemodynamic consequences are described and comparison made to other types of aortic atresia. Cross-sectional echocardiography was found to be reliable in determining both atrioventricular and ventriculo-arterial connections in the presence of aortic atresia and a solitary ventricle.
摘要
一名患有主动脉闭锁且单心室有双入口的男婴，呈现出“左心发育不全综合征”的临床症状。描述了血流动力学后果，并与其他类型的主动脉闭锁进行了比较。发现在存在主动脉闭锁和单心室的情况下，横断面超声心动图在确定房室和心室动脉连接方面是可靠的。
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