Nordenberg D F, Hanna B, Fouron J C, Der Kaloustian V M
Department of Pediatrics, McGill University, Montreal, Quebec, Canada.
Am J Med Genet. 1989 Feb;32(2):182-3. doi: 10.1002/ajmg.1320320208.
We report on two sisters with secundum atrial septal defect, perimembranous ventricular septal defect, and coarctation of the aorta. Identical anatomical malformations were verified by echocardiography and at operation. No other affected relatives were identified. We suggest that this is a specific, possibly recessively inherited type of complex cardiac malformation.
我们报告了两例患有继发孔房间隔缺损、膜周部室间隔缺损和主动脉缩窄的姐妹。超声心动图和手术证实了相同的解剖畸形。未发现其他受影响的亲属。我们认为这是一种特定的、可能隐性遗传的复杂性心脏畸形类型。
