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Please use this identifier to cite or link to this item: http://acervodigital.unesp.br/handle/11449/72878
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dc.contributor.authorOliveira, Camila Ive Ferreira-
dc.contributor.authorFilho, Guaracy Carvalho-
dc.contributor.authorSouza, Antonio Soares-
dc.contributor.authorFett-Conte, Agnes Cristina-
dc.date.accessioned2014-05-27T11:26:15Z-
dc.date.accessioned2016-10-25T18:35:55Z-
dc.date.available2014-05-27T11:26:15Z-
dc.date.available2016-10-25T18:35:55Z-
dc.date.issued2011-12-01-
dc.identifierhttp://www.amjcaserep.com/abstract/index/idArt/882136-
dc.identifier.citationAmerican Journal of Case Reports, v. 12, p. 189-194.-
dc.identifier.issn1941-5923-
dc.identifier.urihttp://hdl.handle.net/11449/72878-
dc.identifier.urihttp://acervodigital.unesp.br/handle/11449/72878-
dc.description.abstractBackground: Spondyloepiphyseal dysplasia-brachydactyly and distinctive speech (SED-BDS) is a syndrome characterized by short stature, disproportionately short limbs, peculiar face, thick and abundant hair, high-pitched and coarse voice, small epiphyses, brachymetacarpalia, brachymetatarsalia and brachy-phalangia of fingers and toes, small pelvis and delayed carpal bone age, among other features. Case Report: We report a Brazilian patient with father, brother and sister presenting with the same typical features of the syndrome. Clinically, he showed disproportionately short stature, rhizo-meso-acromelic shortness of the extremities, short hands and feet, a peculiar distinctive high-pitched voice, peculiar facies, and other features already reported as characteristic of this syndrome. Radiographic fndings included shape anomalies of the vertebral bodies such as cuboid-shaped vertebral bodies, mild scoliosis, short and broad tubular bones, brachymetacarpalia, brachymetatarsalia, and brachy-dactyly, lumbar hyperlordosis, generalized osteopenia, and hypoplastic iliac wings. Conclusions: Few cases have been described, as this is a rare skeletal dysplasia. This paper describes a new familial case of SED-BDS. © The American Journal of Case Reports.en
dc.format.extent189-194-
dc.language.isoeng-
dc.sourceScopus-
dc.subjectFantasy island syndrome-
dc.subjectSED-BDS-
dc.subjectTattoo dysplasia-
dc.subjectadolescent-
dc.subjectbody size-
dc.subjectbone disease-
dc.subjectbone growth-
dc.subjectbrachydactyly-
dc.subjectbrachymetacarpy-
dc.subjectbrachymetatarsalia-
dc.subjectBrazilian-
dc.subjectcase report-
dc.subjectepiphysis-
dc.subjectethnic group-
dc.subjectfamilial disease-
dc.subjectfoot-
dc.subjectgenetic disorder-
dc.subjectgrowth retardation-
dc.subjecthand-
dc.subjecthuman-
dc.subjecthypoplastic iliac wings-
dc.subjectlimb-
dc.subjectlong bone-
dc.subjectlumbar hyperlordosis-
dc.subjectmale-
dc.subjectossification-
dc.subjectosteopenia-
dc.subjectphysical examination-
dc.subjectscoliosis-
dc.subjectshort stature-
dc.subjectspondyloepiphyseal dysplasia brachydactyl and distinctive speech-
dc.subjectvertebra malformation-
dc.titleSED-brachydactyly and distinctive speech: Report of a new familial caseen
dc.typeoutro-
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)-
dc.contributor.institutionFaculdade de Medicina de São José do Rio Preto (FAMERP)-
dc.description.affiliationDepartment of Biology IBILCE/UNESP, São José do Rio Preto, SP-
dc.description.affiliationDepartment of Orthopedics and Traumatology Medical School FAMERP/FUNFARME, São José do Rio Preto, São Paulo-
dc.description.affiliationDepartment of Imaging Medical School FAMERP/FUNFARME, São José do Rio Preto, São Paulo-
dc.description.affiliationDepartment of Molecular Biology Medical School FAMERP/FUNFARME, São José do Rio Preto, São Paulo-
dc.description.affiliationUnespDepartment of Biology IBILCE/UNESP, São José do Rio Preto, SP-
dc.identifier.doi10.12659/AJCR.882136-
dc.rights.accessRightsAcesso restrito-
dc.identifier.file2-s2.0-84855368546.pdf-
dc.relation.ispartofAmerican Journal of Case Reports-
dc.identifier.scopus2-s2.0-84855368546-
Appears in Collections:Artigos, TCCs, Teses e Dissertações da Unesp

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