A rare case with multiple urinary anomalies associated with urethral duplication: Distal hypospadias, posterior urethral valve, left vesicoureteral reflux, and right renal agenesis

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dc.contributor.authorBayram, Salih
dc.contributor.authorBasuguy, Erol
dc.date.accessioned2024-04-24T19:11:30Z
dc.date.available2024-04-24T19:11:30Z
dc.date.issued2019
dc.departmentDicle Üniversitesien_US
dc.description.abstractUrethral duplication is a rare congenital malformation with multiple clinical manifestations. Here, wepresent a case involving a boy with hypospadiac urethral duplication and multiple congenitalanomalies. The patient had additional anomalies including a posterior urethral valve, leftvesicoureteral reflux and right renal agenesis. This case is discussed in terms of the type of urethralduplication and the importance of additional anomalies.en_US
dc.identifier.doi10.14534/j-pucr.2019146687
dc.identifier.endpage4en_US
dc.identifier.issn2148-2969
dc.identifier.issue1en_US
dc.identifier.startpage1en_US
dc.identifier.trdizinid348629
dc.identifier.urihttps://doi.org/10.14534/j-pucr.2019146687
dc.identifier.urihttps://search.trdizin.gov.tr/yayin/detay/348629
dc.identifier.urihttps://hdl.handle.net/11468/28045
dc.identifier.volume6en_US
dc.indekslendigikaynakTR-Dizin
dc.language.isoenen_US
dc.relation.ispartofPediatric Urology Case Reports
dc.relation.publicationcategoryMakale - Ulusal Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.titleA rare case with multiple urinary anomalies associated with urethral duplication: Distal hypospadias, posterior urethral valve, left vesicoureteral reflux, and right renal agenesisen_US
dc.titleA rare case with multiple urinary anomalies associated with urethral duplication: Distal hypospadias, posterior urethral valve, left vesicoureteral reflux, and right renal agenesis
dc.typeArticleen_US

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