Basaran, UNInan, MGücer, FYardim, TPul, M2024-06-122024-06-1220020179-0358https://doi.org/10.1007/s00383-002-0815-2https://hdl.handle.net/20.500.14551/21306Spontaneous prenatal closure of gastroschisis (GS) is rare and usually associated with atresia of the midgut. We describe a case of GS diagnosed at 20 weeks' gestation that resolved spontaneously in utero. At delivery the infant had an ileus. A laparotomy with a jejunocolostomy was performed, but she died at 2 months of age due to complications of total parenteral nutrition.en10.1007/s00383-002-0815-2info:eu-repo/semantics/closedAccessGastroschisisFetal Abdominal-Wall ClosureIntestinal AtresiaShort-Bowel SyndromeVanishing BowelManagementClosureDefectArticle185-6550552Q3WOS:0001795080000702-s2.0-003673075612415410Q2