Double cystic duodenal duplication: A case report and review of the literature

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dc.contributor.authorBalik E.
dc.contributor.authorTaneli C.
dc.date.accessioned2019-10-27T00:33:56Z
dc.date.available2019-10-27T00:33:56Z
dc.date.issued1993
dc.departmentEge Üniversitesien_US
dc.description.abstractDuplications of duodenum are relatively rare congenital abnormalities of the gastrointestinal tract. Although duplications can occur anywhere in the alimentary tract, duodenal duplications are encountered only 5-10% of the total. Up to date, only a single case of double cystic duplication is reported in the literature. A new case of this very uncommon abnormality is present.en_US
dc.identifier.endpage100en_US
dc.identifier.issn1016-5142
dc.identifier.issn1016-5142en_US
dc.identifier.issue02.Maren_US
dc.identifier.scopusqualityN/Aen_US
dc.identifier.startpage99en_US
dc.identifier.urihttps://hdl.handle.net/11454/24158
dc.identifier.volume7en_US
dc.indekslendigikaynakScopusen_US
dc.language.isoenen_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.subjectDouble cystic duplicationen_US
dc.subjectDuodenumen_US
dc.titleDouble cystic duodenal duplication: A case report and review of the literatureen_US
dc.typeArticleen_US

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