Oral manifestations of Albright hereditary osteodystrophy: a case report.

Detalhes bibliográficos
Autor(a) principal: Gomes, Mônica Fernandes
Data de Publicação: 2002
Outros Autores: Camargo, Ana Maria Albernaz, Sampaio, Tatiane Alves, Graziozi, Maria Aparecida O C, Armond, Mônica Costa
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1590/S0041-87812002000400006
http://hdl.handle.net/11449/66919
Resumo: Albright hereditary osteodystrophy is a hereditary metabolic disorder of dominant autosomal etiology that is commonly characterized by short stature, round face, small metacarpus and metatarsus, mental retardation, osteoporosis, subcutaneous calcification, variable hypocalcemia, and hyperphosphatemia. In this study, we report a clinical case of a 17-year-old woman with Albright hereditary osteodystrophy, and we discuss her clinical, radiographic, and laboratory test characteristics together with the oral manifestations, and we correlate them with the characteristics found in the literature. We also discuss the odontological management of treatment of related periodontal disease and planning for corrections of related malocclusions.
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spelling Oral manifestations of Albright hereditary osteodystrophy: a case report.adolescentAlbright syndromecase reportfemalehumanmouth diseasepseudohypoparathyroidismradiographyAdolescentFemaleFibrous Dysplasia, PolyostoticHumansPseudohypoparathyroidismStomatognathic DiseasesAlbright hereditary osteodystrophy is a hereditary metabolic disorder of dominant autosomal etiology that is commonly characterized by short stature, round face, small metacarpus and metatarsus, mental retardation, osteoporosis, subcutaneous calcification, variable hypocalcemia, and hyperphosphatemia. In this study, we report a clinical case of a 17-year-old woman with Albright hereditary osteodystrophy, and we discuss her clinical, radiographic, and laboratory test characteristics together with the oral manifestations, and we correlate them with the characteristics found in the literature. We also discuss the odontological management of treatment of related periodontal disease and planning for corrections of related malocclusions.Universidade Estadual Paulista (Unesp)Gomes, Mônica FernandesCamargo, Ana Maria AlbernazSampaio, Tatiane AlvesGraziozi, Maria Aparecida O CArmond, Mônica Costa2014-05-27T11:20:28Z2014-05-27T11:20:28Z2002-07-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article161-166application/pdfhttp://dx.doi.org/10.1590/S0041-87812002000400006Revista do Hospital das Clinicas de Faculdade de Medicina da Universidade de Sao Paulo, v. 57, n. 4, p. 161-166, 2002.0041-8781http://hdl.handle.net/11449/6691910.1590/S0041-87812002000400006S0041-878120020004000062-s2.0-00366535592-s2.0-0036653559.pdf1274225455678400Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengRevista do Hospital das Clinicas de Faculdade de Medicina da Universidade de Sao Pauloinfo:eu-repo/semantics/openAccess2024-01-05T06:22:16Zoai:repositorio.unesp.br:11449/66919Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T22:09:34.808005Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Oral manifestations of Albright hereditary osteodystrophy: a case report.
title Oral manifestations of Albright hereditary osteodystrophy: a case report.
spellingShingle Oral manifestations of Albright hereditary osteodystrophy: a case report.
Gomes, Mônica Fernandes
adolescent
Albright syndrome
case report
female
human
mouth disease
pseudohypoparathyroidism
radiography
Adolescent
Female
Fibrous Dysplasia, Polyostotic
Humans
Pseudohypoparathyroidism
Stomatognathic Diseases
title_short Oral manifestations of Albright hereditary osteodystrophy: a case report.
title_full Oral manifestations of Albright hereditary osteodystrophy: a case report.
title_fullStr Oral manifestations of Albright hereditary osteodystrophy: a case report.
title_full_unstemmed Oral manifestations of Albright hereditary osteodystrophy: a case report.
title_sort Oral manifestations of Albright hereditary osteodystrophy: a case report.
author Gomes, Mônica Fernandes
author_facet Gomes, Mônica Fernandes
Camargo, Ana Maria Albernaz
Sampaio, Tatiane Alves
Graziozi, Maria Aparecida O C
Armond, Mônica Costa
author_role author
author2 Camargo, Ana Maria Albernaz
Sampaio, Tatiane Alves
Graziozi, Maria Aparecida O C
Armond, Mônica Costa
author2_role author
author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
dc.contributor.author.fl_str_mv Gomes, Mônica Fernandes
Camargo, Ana Maria Albernaz
Sampaio, Tatiane Alves
Graziozi, Maria Aparecida O C
Armond, Mônica Costa
dc.subject.por.fl_str_mv adolescent
Albright syndrome
case report
female
human
mouth disease
pseudohypoparathyroidism
radiography
Adolescent
Female
Fibrous Dysplasia, Polyostotic
Humans
Pseudohypoparathyroidism
Stomatognathic Diseases
topic adolescent
Albright syndrome
case report
female
human
mouth disease
pseudohypoparathyroidism
radiography
Adolescent
Female
Fibrous Dysplasia, Polyostotic
Humans
Pseudohypoparathyroidism
Stomatognathic Diseases
description Albright hereditary osteodystrophy is a hereditary metabolic disorder of dominant autosomal etiology that is commonly characterized by short stature, round face, small metacarpus and metatarsus, mental retardation, osteoporosis, subcutaneous calcification, variable hypocalcemia, and hyperphosphatemia. In this study, we report a clinical case of a 17-year-old woman with Albright hereditary osteodystrophy, and we discuss her clinical, radiographic, and laboratory test characteristics together with the oral manifestations, and we correlate them with the characteristics found in the literature. We also discuss the odontological management of treatment of related periodontal disease and planning for corrections of related malocclusions.
publishDate 2002
dc.date.none.fl_str_mv 2002-07-01
2014-05-27T11:20:28Z
2014-05-27T11:20:28Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1590/S0041-87812002000400006
Revista do Hospital das Clinicas de Faculdade de Medicina da Universidade de Sao Paulo, v. 57, n. 4, p. 161-166, 2002.
0041-8781
http://hdl.handle.net/11449/66919
10.1590/S0041-87812002000400006
S0041-87812002000400006
2-s2.0-0036653559
2-s2.0-0036653559.pdf
1274225455678400
url http://dx.doi.org/10.1590/S0041-87812002000400006
http://hdl.handle.net/11449/66919
identifier_str_mv Revista do Hospital das Clinicas de Faculdade de Medicina da Universidade de Sao Paulo, v. 57, n. 4, p. 161-166, 2002.
0041-8781
10.1590/S0041-87812002000400006
S0041-87812002000400006
2-s2.0-0036653559
2-s2.0-0036653559.pdf
1274225455678400
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Revista do Hospital das Clinicas de Faculdade de Medicina da Universidade de Sao Paulo
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 161-166
application/pdf
dc.source.none.fl_str_mv Scopus
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv
_version_ 1808129398873784320

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