An uncommon association of cloacal malformation with Hirschsprung's Disease, congenital pouch colon and vaginal duplication

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dc.contributor.authorDokucu A.I.
dc.contributor.authorÖztürk H.
dc.contributor.authorBükte Y.
dc.contributor.authorAzal Ö.F.
dc.date.accessioned2024-04-24T17:58:44Z
dc.date.available2024-04-24T17:58:44Z
dc.date.issued2001
dc.departmentDicle Üniversitesien_US
dc.description.abstractCloacal 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.en_US
dc.identifier.endpage84en_US
dc.identifier.issn1016-5142
dc.identifier.issue2en_US
dc.identifier.scopus2-s2.0-0035708613en_US
dc.identifier.scopusqualityN/Aen_US
dc.identifier.startpage81en_US
dc.identifier.urihttps://hdl.handle.net/11468/24078
dc.identifier.volume15en_US
dc.indekslendigikaynakScopus
dc.language.isotren_US
dc.relation.ispartofPediatrik Cerrahi Dergisien_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectCloacal Malformationen_US
dc.subjectCongenital Pouch Colonen_US
dc.subjectHirschsprung's Diseaseen_US
dc.subjectVaginal Duplicationen_US
dc.titleAn uncommon association of cloacal malformation with Hirschsprung's Disease, congenital pouch colon and vaginal duplicationen_US
dc.title.alternativeKloakal anomalinin Hirschsprung hastali?i, do?umsal 'pouch' kolon ve vajinal duplikasyon ile seyreden nadir birlikteligien_US
dc.typeArticleen_US

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