CONGENITAL IMPERFORATE HYMEN WITH BILATERAL HYDRONEPHROSIS, POLYDACTYLY AND LARYNGOCELE: A Rare Neonatal Presentation

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dc.contributor.authorÖztürk, Hülya
dc.contributor.authorYazıcı, Burhan
dc.contributor.authorKüçük, Adem
dc.contributor.authorŞenses, Dursun Ali
dc.date.accessioned2020-04-30T22:41:38Z
dc.date.available2020-04-30T22:41:38Z
dc.date.issued2010
dc.departmentDÜ, Tıp Fakültesi, Cerrahi Tıp Bilimleri Bölümüen_US
dc.descriptionWOS: 000275954100004en_US
dc.descriptionPubMed: 20334483en_US
dc.description.abstractImperforate hymen is a rare congenital malformation to present with symptoms in the neonatal period. We present a case of a 5-day-old neonate with a marked interlabial swelling causing urinary retention. Imaging revealed hydrometrocolpos, hydrosalpinx, and bilateral hydronephrosis. Additionally, our patient had polydactyly of both feet and hands, and laryngocele that have not been previously described in literature. Hymenectomy is the mainstay of management to prevent the development of hematocolpos, pain, and possible retrograde menstruation.</.en_US
dc.identifier.doi10.3109/15513811003620609en_US
dc.identifier.endpage94en_US
dc.identifier.issn1551-3815
dc.identifier.issn1551-3823
dc.identifier.issue2en_US
dc.identifier.scopusqualityQ3en_US
dc.identifier.startpage89en_US
dc.identifier.urihttps://doi.org/10.3109/15513811003620609
dc.identifier.urihttps://hdl.handle.net/20.500.12684/3223
dc.identifier.volume29en_US
dc.identifier.wosWOS:000275954100004en_US
dc.identifier.wosqualityQ4en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakPubMeden_US
dc.indekslendigikaynakScopusen_US
dc.language.isoenen_US
dc.publisherTaylor & Francis Incen_US
dc.relation.ispartofFetal And Pediatric Pathologyen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectNeonateen_US
dc.subjecthydometrocolposen_US
dc.subjectimperforate hymenen_US
dc.subjectpolydactylyen_US
dc.titleCONGENITAL IMPERFORATE HYMEN WITH BILATERAL HYDRONEPHROSIS, POLYDACTYLY AND LARYNGOCELE: A Rare Neonatal Presentationen_US
dc.typeArticleen_US

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