Dokucu A.I.Öztürk H.Bükte Y.Azal Ö.F.2024-04-242024-04-2420011016-5142https://hdl.handle.net/11468/24078Cloacal malformations are characterized by a single opening that connects the urinary tract, the internal genitalia and the intestinal tract via a urogenital sinus. We describe the first reported case of a cloacal malformation consisting of congenital pouch colon associated with Hirschsprung's Disease and vaginal duplication in a 13 year-old girl. We also discussed the method of surgical treatment performed in this girl. To plan reconstruction for an individual case with cloaca, the surgeon should be acquainted with associated anomalies and a wide range of anatomy that may be present.trinfo:eu-repo/semantics/closedAccessCloacal MalformationCongenital Pouch ColonHirschsprung's DiseaseVaginal DuplicationAn uncommon association of cloacal malformation with Hirschsprung's Disease, congenital pouch colon and vaginal duplicationKloakal anomalinin Hirschsprung hastali?i, do?umsal 'pouch' kolon ve vajinal duplikasyon ile seyreden nadir birlikteligiArticle15281842-s2.0-0035708613N/A