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Duodenal atresiaDefinition Duodenal atresia is a condition in which the duodenum (the first part of the small bowel) has not developed properly. It is not open and cannot allow the passage of stomach contents. Causes, incidence, and risk factors The cause of duodenal atresia is unknown, but it is thought to result from problems during the developmental stage in which the embryo's duodenum normally changes from solid to tube-like (recanalization). Duodenal atresia is present in more than 1 in 10,000 live births. Approximately 20-30% of infants with duodenal atresia have Downs syndrome. Duodenal atresia is often associated with other congenital abnormalities. Symptoms
Signs and tests
Treatment A tube is placed to decompress the stomach. Dehydration and electrolyte abnormalities are corrected by providing fluids through an intravenous tube. An evaluation for other congenital anomalies should be performed. Surgery to correct the duodenal blockage is necessary, but is not an emergency. The surgical approach will depend on the nature of the abnormality. Associated problems (such as those related to Downs syndrome) must be treated as appropriate. Expectations (prognosis) Recovery from the duodenal atresia is expected after treatment. Untreated, the condition is fatal. Complications
Calling your health care provider Call your health care provider if your newborn is feeding poorly or not at all, vomiting (not simply spitting up), not urinating or stooling, or if the vomit is green. Prevention There is no known prevention. Illustrations
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