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OHVIRA Syndrome with a Blind-Ended Ureteral Remnant

dc.contributor.authorSousa, R
dc.contributor.authorAmante, S
dc.contributor.authorCarneiro, R
dc.contributor.authorNunes, A
dc.contributor.authorSoares, E
dc.date.accessioned2022-08-10T13:44:08Z
dc.date.available2022-08-10T13:44:08Z
dc.date.issued2020
dc.description.abstractOHVIRA syndrome is characterized by a didelphys uterus with an obstructed/blind hemi-vagina and ipsilateral renal agenesis. We presented a case of a female child with a pre-natal diagnosis of left renal agenesis whose post-natal imaging findings were consistent with OHVIRA syndrome.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationActa Radiol Port. 2020; 32(2): 35-36pt_PT
dc.identifier.urihttp://hdl.handle.net/10400.17/4197
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherSociedade Portuguesa de Radiologia e Medicina Nuclearpt_PT
dc.subjectOHVIRA syndromept_PT
dc.subjectMullerian malformationspt_PT
dc.subjectCongenital female genital tract anomaliespt_PT
dc.subjectHDE IMApt_PT
dc.titleOHVIRA Syndrome with a Blind-Ended Ureteral Remnantpt_PT
dc.title.alternativeSíndrome OHVIRA com Remanescente Uretéricopt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPage36pt_PT
oaire.citation.issue2pt_PT
oaire.citation.startPage35pt_PT
oaire.citation.volume32pt_PT
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT

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