Publication
OHVIRA Syndrome with a Blind-Ended Ureteral Remnant
dc.contributor.author | Sousa, R | |
dc.contributor.author | Amante, S | |
dc.contributor.author | Carneiro, R | |
dc.contributor.author | Nunes, A | |
dc.contributor.author | Soares, E | |
dc.date.accessioned | 2022-08-10T13:44:08Z | |
dc.date.available | 2022-08-10T13:44:08Z | |
dc.date.issued | 2020 | |
dc.description.abstract | OHVIRA 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.version | info:eu-repo/semantics/publishedVersion | pt_PT |
dc.identifier.citation | Acta Radiol Port. 2020; 32(2): 35-36 | pt_PT |
dc.identifier.uri | http://hdl.handle.net/10400.17/4197 | |
dc.language.iso | eng | pt_PT |
dc.peerreviewed | yes | pt_PT |
dc.publisher | Sociedade Portuguesa de Radiologia e Medicina Nuclear | pt_PT |
dc.subject | OHVIRA syndrome | pt_PT |
dc.subject | Mullerian malformations | pt_PT |
dc.subject | Congenital female genital tract anomalies | pt_PT |
dc.subject | HDE IMA | pt_PT |
dc.title | OHVIRA Syndrome with a Blind-Ended Ureteral Remnant | pt_PT |
dc.title.alternative | Síndrome OHVIRA com Remanescente Uretérico | pt_PT |
dc.type | journal article | |
dspace.entity.type | Publication | |
oaire.citation.endPage | 36 | pt_PT |
oaire.citation.issue | 2 | pt_PT |
oaire.citation.startPage | 35 | pt_PT |
oaire.citation.volume | 32 | pt_PT |
rcaap.rights | openAccess | pt_PT |
rcaap.type | article | pt_PT |