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Use este identificador para citar ou linkar para este item: https://repositorio.ufba.br/handle/ri/5016
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dc.contributor.authorPinheiro, Antonio Luiz Barbosa-
dc.contributor.authorAraújo, Luciana Cavalcanti-
dc.contributor.authorOliveira, Suely Baptista-
dc.contributor.authorSampaio, Maria Carmeli Correia-
dc.contributor.authorFreitas, André Carlos-
dc.creatorPinheiro, Antonio Luiz Barbosa-
dc.creatorAraújo, Luciana Cavalcanti-
dc.creatorOliveira, Suely Baptista-
dc.creatorSampaio, Maria Carmeli Correia-
dc.creatorFreitas, André Carlos-
dc.date.accessioned2012-01-03T22:47:48Z-
dc.date.available2012-01-03T22:47:48Z-
dc.date.issued2003-
dc.identifier.issn1806-4760-
dc.identifier.urihttp://www.repositorio.ufba.br/ri/handle/ri/5016-
dc.descriptionp.67-70pt_BR
dc.description.abstractGoldenhar’s syndrome is a rare condition described initially in the early 1950’s. It is characterized by a combination of anomalies: dermal epibulbar cysts, auricular appendices and malformation of the ears. In 1963, Gorlin suggested the name oculo-auriculovertebral (OAV) dysplasia for this condition and also included vertebral anomalies as signs of the syndrome. The etiology of this rare disease is not fully understood, as it has shown itself variable genetically and of unclear causes. This work reports a case of Goldenhar’s syndrome in an 11-year-old female, who presented all classical signs of this rare conditionpt_BR
dc.language.isoenpt_BR
dc.subjectdeformitypt_BR
dc.subjectmanifestationpt_BR
dc.subjectoculo-auriculo-vertebral displasiapt_BR
dc.titleGoldenhar’s Syndrome - Case Reportpt_BR
dc.title.alternativeBrazilian Dental Journalpt_BR
dc.typeArtigo de Periódicopt_BR
dc.identifier.number14(1)pt_BR
Aparece nas coleções:Artigo Publicado em Periódico (Faculdade de Odontologia)

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