Early abdomino-perineal pull-through vaginoplasty

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dc.contributor.authorCiftci I.
dc.contributor.authorTastekin A.
dc.contributor.authorAnnagur A.
dc.contributor.authorKoplay M.
dc.date.accessioned2020-03-26T18:48:12Z
dc.date.available2020-03-26T18:48:12Z
dc.date.issued2013
dc.departmentSelçuk Üniversitesien_US
dc.description.abstractVaginal agenesis is known as one of the Müllerian anomalies. Müllerian anomalies occur during gonadal development and differentiation, and may lead to complex outcomes. McKusick-Kaufman syndrome (MKS) is an autosomal recessive multiple malformation syndrome characterized by Müllerian anomalies with hydrometrocolpos (HMC) and postaxial polydactyly (PAP). We report a case of a female newborn that developed hydronephrosis and respiratory distress due to compression of the cystic mass and underwent surgery on postpartum day 3. Pull-through vaginoplasty was performed with an abdomino-perineal approach. We report the unique treatment approach in this case.en_US
dc.identifier.doi10.4103/0189-6725.115053en_US
dc.identifier.endpage191en_US
dc.identifier.issn0189-6725en_US
dc.identifier.issue2en_US
dc.identifier.pmid23860075en_US
dc.identifier.scopusqualityQ4en_US
dc.identifier.startpage188en_US
dc.identifier.urihttps://dx.doi.org/10.4103/0189-6725.115053
dc.identifier.urihttps://hdl.handle.net/20.500.12395/30132
dc.identifier.volume10en_US
dc.indekslendigikaynakScopusen_US
dc.indekslendigikaynakPubMeden_US
dc.language.isoenen_US
dc.relation.ispartofAfrican Journal of Paediatric Surgeryen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.selcuk20240510_oaigen_US
dc.subjectCongenitalen_US
dc.subjecthydrometrocolposen_US
dc.subjectMcKusick-Kaufman syndromeen_US
dc.subjectneonateen_US
dc.subjectpolydactylyen_US
dc.subjectpull-throughen_US
dc.subjectvaginoplastyen_US
dc.titleEarly abdomino-perineal pull-through vaginoplastyen_US
dc.typeArticleen_US

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