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Familial duodenal atresia: a report of two siblings.

The familial occurrence of duodenal atresia is extremely uncommon. The author reports duodenal atresia occurring in two siblings who underwent successful surgical repair at the Pediatric Surgical Unit, Department of Surgery, Ratchaburi Hospital. To the author's knowledge, this is the first report of familial duodenal atresia in Thailand.

Duodenal Obstruction↗

Acquired biliary atresia.

Three infants are described in whom acquired biliary atresia developed during the perinatal period. In two cases this was related to a spontaneous perforation of the bile duct, and in the other it probably was related to previous surgery for duodenal and ileal atresias. Clinically, the symptoms in these patients differed from the congenital forms of biliary atresia; two of the infants had dilated intrahepatic ducts on ultrasonography, and all had restriction of disease to the extrahepatic bile ducts and an excellent response to surgery.

Bile Duct Diseases↗