Albright's syndrome: review of the literature and case report.

dc.contributorUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-27T11:17:58Z
dc.date.accessioned2022-10-05T17:29:39Z
dc.date.available2014-05-27T11:17:58Z
dc.date.available2022-10-05T17:29:39Z
dc.date.created2014-05-27T11:17:58Z
dc.date.issued1994-12-01
dc.identifierThe Journal of Nihon University School of Dentistry, v. 36, n. 4, p. 283-287, 1994.
dc.identifier0029-0432
dc.identifierhttp://hdl.handle.net/11449/64525
dc.identifier10.2334/josnusd1959.36.283
dc.identifier2-s2.0-0028707973
dc.identifier7650237459252010
dc.identifier8029177169916525
dc.identifier3113606866386377
dc.identifier2323089849082516
dc.identifier0000-0002-3185-2826
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/3914554
dc.description.abstractAlbright's syndrome is characterized by the presence of polyostotic fibrous dysplasia, endocrinopathies and brown spots on the skin. In the present article the authors describe a case occurring in a 20-year-old female patient, who is currently being followed radiographically after a mandibular bone biopsy.
dc.languageeng
dc.relationThe Journal of Nihon University School of Dentistry
dc.rightsAcesso aberto
dc.sourceScopus
dc.subjectadult
dc.subjectAlbright syndrome
dc.subjectcase report
dc.subjectface asymmetry
dc.subjectfemale
dc.subjectfollow up
dc.subjectfrontal bone
dc.subjecthuman
dc.subjecthyperpigmentation
dc.subjectjaw disease
dc.subjectpathology
dc.subjectreview
dc.subjectAdult
dc.subjectCase Report
dc.subjectFacial Asymmetry
dc.subjectFemale
dc.subjectFibrous Dysplasia, Polyostotic
dc.subjectFollow-Up Studies
dc.subjectFrontal Bone
dc.subjectHuman
dc.subjectHyperpigmentation
dc.subjectMandibular Diseases
dc.titleAlbright's syndrome: review of the literature and case report.
dc.typeArtigo


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