Inanç I.Kizilkaya O.Başaran U.N.Avlan D.2024-06-122024-06-1220181305-5194https://doi.org/10.5222/JTAPS.2018.050https://search.trdizin.gov.tr/yayin/detay/329308https://hdl.handle.net/20.500.14551/16865A newborn who had been followed up by another center with the diagnosis of antenatal polyhydroamniosis was referred to our hospital because of detection of anal atresia and inability to insert a nasogastric tube. A contrast radiography was performed and an esophageal atretic pouch was detected. Visualization of a double bubble sign also established the diagnosis of duodenal atresia. Since the patient's birth week and birth weight was suitable; through laparatomy incision gastrojejunostomy was performed and sigmoid diverting colostomy was opened. Then, right thoracotomy was performed, and tracheaesophageal fistula was closed, and finally end-to-end esophageal anastomosis was realized to treat esophageal atresia. Our case is a rare example of isochronous anomalies of gastrointestinal system and we also aim to analyze alternatives, and challenges concerning diagnosis and treatment. 2017 © Logos Medical Publishing. All Rights Reserved.tr10.5222/JTAPS.2018.050info:eu-repo/semantics/closedAccessAnal Atresia; Duodenal Atresia; Esophageal Atresia; NewbornArticle32150532-s2.0-85072808343Q4329308