Blind ending ureter: A rarely diagnosed ureteral duplication anomaly in childhood

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dc.contributor.authorBalasar M.
dc.contributor.authorPişkin M.M.
dc.contributor.authorÇiçekçi F.
dc.contributor.authorGürbüz R.
dc.date.accessioned2020-03-26T18:05:58Z
dc.date.available2020-03-26T18:05:58Z
dc.date.issued2010
dc.departmentSelçuk Üniversitesien_US
dc.description.abstractBlind ending ureter is a rare congenital malformation of the urinary system and is classified as a ureteral duplication anomaly. Most cases are not diagnosed until they become symptomatic. Although it is a congenital malformation, patients are usually diagnosed in the 3rd and 4th decades and presentation in childhood is very rare. Mostly they manifest with loin pain, urinary tract infection, or stone disease. Intravenous pyelogram, retrograde pyelogram, and computerized tomography can be used for diagnosis. Voiding cystourethrography must be performed to exclude associated vesicoureteral reflux. Herein, we report an 11-year-old child who had a blind ending duplicated ureter associated with vesicoureteral reflux causing renal atrophy.en_US
dc.identifier.endpage85en_US
dc.identifier.issn1300056Xen_US
dc.identifier.issue2en_US
dc.identifier.scopusqualityN/Aen_US
dc.identifier.startpage84en_US
dc.identifier.urihttps://hdl.handle.net/20.500.12395/25586
dc.identifier.volume21en_US
dc.indekslendigikaynakScopusen_US
dc.language.isoenen_US
dc.relation.ispartofGazi Medical Journalen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.selcuk20240510_oaigen_US
dc.subjectBlind ending ureteren_US
dc.subjectUreteren_US
dc.subjectUrogenital abnormalityen_US
dc.subjectVesicoureteral refluxen_US
dc.titleBlind ending ureter: A rarely diagnosed ureteral duplication anomaly in childhooden_US
dc.typeArticleen_US

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