双心室心肌致密化不全：胎儿窘迫和三尖瓣反流的罕见原因。
Biventricular noncompaction: A rare cause of fetal distress and tricuspid regurgitation.
作者信息
Tomar M, Radhakrishnan S
机构信息
Department of Pediatrics and Congenital Heart Diseases, Escorts Heart Institute & Research Centre, New Delhi, India.
出版信息
Images Paediatr Cardiol. 2009 Oct;11(4):1-5.
Abstract
Isolated noncompaction of the ventricular myocardium involving both ventricles is a rare entity. Here we report a rare case of biventricular noncompaction presenting with features of fetal distress and moderate tricuspid regurgitation. Noncompaction of both ventricles was diagnosed at birth.
摘要
累及双心室的孤立性心室心肌致密化不全是一种罕见的病症。在此，我们报告一例罕见的双心室致密化不全病例，该病例表现为胎儿窘迫和中度三尖瓣反流。出生时诊断为双心室致密化不全。
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