Nir A, Weintraub Z, Oliven A, Kelener J, Lurie M
Department of Pediatrics, Carmel Hospital, Haifa, Israel.
Pediatr Cardiol. 1990 Oct;11(4):208-10. doi: 10.1007/BF02238368.
An infant, born to a mother on carbamazepine monotherapy, had a complex cardiac anomaly, consisting of double-outlet right ventricle (DORV), right-sided aorta, pulmonary artery hypoplasia, left ventricular endocardial fibroelastosis, and anatomic evidence of a spontaneously closed muscular ventricular septal defect (VSD). The last finding is one which, to the best of our knowledge, has never been illustrated before.
一名母亲接受卡马西平单药治疗的婴儿患有复杂心脏畸形，包括右心室双出口（DORV）、右侧主动脉、肺动脉发育不全、左心室心内膜弹力纤维增生症，以及存在一个自发闭合的肌部室间隔缺损（VSD）的解剖学证据。据我们所知，最后一项发现此前从未有过相关例证。
