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Case Report: Septate Uterus in a Girl with Rubinstein–Taybi Syndrome

dc.contributor.authorCoellho, Filipa de Castro
dc.contributor.authorCâmara, Sara
dc.contributor.authorAlves, Inés
dc.contributor.authorBrazão, Kathleen
dc.date.accessioned2019-03-12T10:21:30Z
dc.date.available2019-03-12T10:21:30Z
dc.date.issued2018-04
dc.description.abstractRubinstein–Taybi syndrome is an extremely rare plurimalformative condition that can affect any organ. However, reports regarding gynecological problems are unusual. We report the first case of a septate uterus in an adolescent with this syndrome, in agreement with the American Society for Reproductive Medicine (ASRM) and the Congenital Uterine Malformations by Expert (CUME) criteria for uterine septum. Additional studies are required to determine whether there is an increased frequency of m¨ullerian duct anomalies with the condition. Our report extends the data on the clinical phenotype associated with Rubinstein–Taybi syndrome.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationde Castro Coelho, F., Câmara, S., Alves, I., & Brazão, K. (2018). Septate Uterus in a Girl with Rubinstein–Taybi Syndrome. Case Reports in Pediatrics, 2018.pt_PT
dc.identifier.doihttps://doi.org/10.1155/2018/7878156pt_PT
dc.identifier.urihttp://hdl.handle.net/10400.26/28048
dc.language.isoengpt_PT
dc.publisherUniversity of Leicesterpt_PT
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/pt_PT
dc.subjectSeptate Uteruspt_PT
dc.subjectRubinstein-Taybi Syndromept_PT
dc.subjectMullerian Duct Anomaliespt_PT
dc.subjectMadeirapt_PT
dc.subjectPortugalpt_PT
dc.subjectMalformações Congenitas Uterinaspt_PT
dc.titleCase Report: Septate Uterus in a Girl with Rubinstein–Taybi Syndromept_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPage4pt_PT
oaire.citation.startPage1pt_PT
oaire.citation.titleCase Reports in Pediatricspt_PT
oaire.citation.volume2018pt_PT
person.familyNamede Castro Coellho
person.givenNameFilipa
person.identifier.orcid0000-0002-8790-0743
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT
relation.isAuthorOfPublicationb866151d-2a4b-42a4-b8df-724fce1a74cb
relation.isAuthorOfPublication.latestForDiscoveryb866151d-2a4b-42a4-b8df-724fce1a74cb

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