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: Relatório
Idioma: eng
Título da fonte: Revista do Hospital das Clínicas
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0041-87812002000400006
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 reportAlbright's hereditary osteodystrophyPseudohypoparathyroidismGs proteinParathormoneOral manifestationsAlbright 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.Faculdade de Medicina / Universidade de São Paulo - FM/USP2002-08-01info:eu-repo/semantics/reportinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0041-87812002000400006Revista do Hospital das Clínicas v.57 n.4 2002reponame:Revista do Hospital das Clínicasinstname:Universidade de São Paulo (USP)instacron:USP10.1590/S0041-87812002000400006info:eu-repo/semantics/openAccessGomes,Mônica FernandesCamargo,Ana Maria AlbernazSampaio,Tatiane AlvesGraziozi,Maria Aparecida O. C.Armond,Mônica Costaeng2002-09-11T00:00:00Zoai:scielo:S0041-87812002000400006Revistahttp://www.scielo.br/rhcPUBhttps://old.scielo.br/oai/scielo-oai.php||revista.hc@hcnet.usp.br1678-99030041-8781opendoar:2002-09-11T00:00Revista do Hospital das Clínicas - Universidade de São Paulo (USP)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
Albright's hereditary osteodystrophy
Pseudohypoparathyroidism
Gs protein
Parathormone
Oral manifestations
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.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 Albright's hereditary osteodystrophy
Pseudohypoparathyroidism
Gs protein
Parathormone
Oral manifestations
topic Albright's hereditary osteodystrophy
Pseudohypoparathyroidism
Gs protein
Parathormone
Oral manifestations
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 2002-08-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/report
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format report
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0041-87812002000400006
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0041-87812002000400006
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S0041-87812002000400006
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Faculdade de Medicina / Universidade de São Paulo - FM/USP
publisher.none.fl_str_mv Faculdade de Medicina / Universidade de São Paulo - FM/USP
dc.source.none.fl_str_mv Revista do Hospital das Clínicas v.57 n.4 2002
reponame:Revista do Hospital das Clínicas
instname:Universidade de São Paulo (USP)
instacron:USP
instname_str Universidade de São Paulo (USP)
instacron_str USP
institution USP
reponame_str Revista do Hospital das Clínicas
collection Revista do Hospital das Clínicas
repository.name.fl_str_mv Revista do Hospital das Clínicas - Universidade de São Paulo (USP)
repository.mail.fl_str_mv ||revista.hc@hcnet.usp.br
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