Combined duodenal and jejunal atresia is extremely uncommon. The famil
iar occurrence of congenital duodenal and small bowel atresia is even
more unusual. To the authors' knowledge, this is the first report of t
wo siblings with simultaneous duodenal and jejunal atresia who underwe
nt successful surgical repair. The report may support the genetic orig
in of some forms of high intestinal atresia. Copyright (C) 1996 by W.B
. Saunders Company