Please use this identifier to cite or link to this item: https://repositorio.unifesp.br/handle/11600/35345
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dc.contributor.authorMoreira Rios, Livia Teresa
dc.contributor.authorAraujo Junior, Edward [UNIFESP]
dc.contributor.authorMachado Nardozza, Luciano Marcondes [UNIFESP]
dc.contributor.authorBruns, Rafael Frederico
dc.contributor.authorMoron, Antonio Fernandes [UNIFESP]
dc.contributor.authorMartins, Marilia da Gloria
dc.date.accessioned2016-01-24T14:27:48Z-
dc.date.available2016-01-24T14:27:48Z-
dc.date.issued2012-10-01
dc.identifierhttp://dx.doi.org/10.1007/s10396-012-0374-7
dc.identifier.citationJournal of Medical Ultrasonics. Tokyo: Springer Japan Kk, v. 39, n. 4, p. 287-289, 2012.
dc.identifier.issn1346-4523
dc.identifier.urihttp://repositorio.unifesp.br/handle/11600/35345-
dc.description.abstractNager syndrome or acrofacial dysostosis is a rare and complex malformation characterized by ear anomalies, micrognathia, radial limb hypoplasia, and absence of the thumb or other fingers. Since the original description of the syndrome in 1948, there have only been four reports of prenatal diagnoses in the literature, all during the second trimester, and only two of them had anatomopathological correlations. We describe a case of Nager syndrome that was suspected in the third trimester of gestation and confirmed postnatally through pathology. the mother was white, 27 years old, and G5P2A2, with a family history of a brother with a harelip. She was referred to our service at 33 weeks of pregnancy with an ultrasound fetal diagnosis of musculoskeletal dysplasia associated with severe micrognathia and severe polyhydramnios. Birth was by means of cesarean section because of suspected fetal distress, which resulted in extraction of a live male fetus with Apgar 1/4, weight of 1,505 g, severe mandibular hypoplasia, low-set ears, severe upper-limb shortening, and absent left thumb. Death occurred 4 h after birth. Anatomopathological examination confirmed the diagnosis of Nager syndrome.en
dc.format.extent287-289
dc.language.isoeng
dc.publisherSpringer
dc.relation.ispartofJournal of Medical Ultrasonics
dc.rightsAcesso restrito
dc.subjectPrenatal diagnosisen
dc.subjectNager syndromeen
dc.subjectUltrasounden
dc.subjectPathologyen
dc.titlePrenatal diagnosis of Nager syndrome in the third trimester of pregnancy and anatomopathological correlationen
dc.typeArtigo
dc.rights.licensehttp://www.springer.com/open+access/authors+rights?SGWID=0-176704-12-683201-0
dc.contributor.institutionUniversidade Federal de São Paulo (UNIFESP)
dc.contributor.institutionFed Univ Maranhao UFMA
dc.contributor.institutionUniversidade Federal do Paraná (UFPR)
dc.description.affiliationFed Univ São Paulo UNIFESP, Dept Obstet, BR-05303000 São Paulo, Brazil
dc.description.affiliationFed Univ Maranhao UFMA, Univ Hosp, Mother Child Unit, Sao Luis, MA, Brazil
dc.description.affiliationFed Univ Parana UFPR, Dept Gynecol & Obstet, Curitiba, Parana, Brazil
dc.description.affiliationUnifespFed Univ São Paulo UNIFESP, Dept Obstet, BR-05303000 São Paulo, Brazil
dc.identifier.doi10.1007/s10396-012-0374-7
dc.description.sourceWeb of Science
dc.identifier.wosWOS:000309862100016
Appears in Collections:Artigo

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