Duodenal Atresia with Bifid Common Bile Duct

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A female infant carried a late pre-natal diagnosis of duodenal atresia that was detected via ultrasound at 38 weeks showing a dilated fetal stomach. The patient was born to an otherwise healthy primagravid mother with a history of Hashimoto’s hypothyroism treated with daily synthroid. The pregnancy and subsequent delivery were uncomplicated, and prior amniocentesis found a 46XX karyotype. At birth, the patient had an abdominal x-ray that showed a distended stomach. The remainder of the abdomen was gasless.

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