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Duodenal Atresia
DefinitionDefinition of Duodenal Atresia Duodenal atresia is the congenital absence or complete closure of a portion of the lumen of the duodenum. SymptomsSymptoms of Duodenal Atresia
CausesCauses of Duodenal Atresia The cause of duodenal atresia is unknown, but it is thought to result from problems during an embryo's development in which the duodenum does not normally change from a solid to a tube-like structure. Duodenal atresia is seen in more than 1 in 10,000 live births. Approximately 20-30% of infants with duodenal atresia have Down syndrome. Duodenal atresia is often associated with other birth defects. DiagnosisDiagnosis of Duodenal Atresia The diagnosis of duodenal atresia is usually confirmed by radiography. An X-ray of the abdomen shows two large air filled spaces, the so-called "double bubble" sign. The air is trapped in the stomach and proximal duodenum. Since the closure of the duodenum is complete in duodenal atresia, no air is seen in the distal duodenum. TreatmentTreatment of Duodenal Atresia The only treatment for duodenal atresia is surgery, which is usually done shortly after birth. Prior to surgery, a nasogastric (NG) tube will be placed in the baby’s stomach to drain the excess fluid and air that have accumulated, and the baby will get an IV so that he can receive fluids that will prevent dehydration. Your pediatrician and surgeon will discuss your baby’s prognosis and care plan with you prior to surgery. Infants with other birth defects or other underlying conditions may not do as well as infants that only have duodenal atresia. Most infants do extremely well after surgery and completely recover from this birth defect. PrognosisPrognosis of Duodenal Atresia Recovery from the duodenal atresia is expected after treatment. Untreated, the condition is deadly. Find Diseases Alphabetically
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