Albright hereditary osteodystrophy: dental management case report
Autor(a) principal: | |
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Data de Publicação: | 2018 |
Outros Autores: | , |
Tipo de documento: | Relatório |
Idioma: | eng |
Título da fonte: | RGO - Revista Gaúcha de Odontologia (Online) |
Texto Completo: | http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1981-86372018000100106 |
Resumo: | ABSTRACT Albright hereditary osteodystrophy is a disorder comprising phenotypic characteristics of genetic origin, such as short stature, obesity, and brachydactyly. It is a rare disorder and is related to pseudohypoparathyroidism. Within dentistry, it may be associated with enamel hypoplasia and late eruption. Furthermore, due to neurological problems, these patients may impose behavioural difficulties during dental appointments. The present study aims to describe the case of a patient with a possible diagnosis of Albright hereditary osteodystrophy, presenting symptoms and limitations to dental management. |
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Albright hereditary osteodystrophy: dental management case reportDental careOral manifestationsPseudohypoparathyroidism.ABSTRACT Albright hereditary osteodystrophy is a disorder comprising phenotypic characteristics of genetic origin, such as short stature, obesity, and brachydactyly. It is a rare disorder and is related to pseudohypoparathyroidism. Within dentistry, it may be associated with enamel hypoplasia and late eruption. Furthermore, due to neurological problems, these patients may impose behavioural difficulties during dental appointments. The present study aims to describe the case of a patient with a possible diagnosis of Albright hereditary osteodystrophy, presenting symptoms and limitations to dental management.Faculdade São Leopoldo Mandic2018-01-01info:eu-repo/semantics/reportinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S1981-86372018000100106RGO - Revista Gaúcha de Odontologia v.66 n.1 2018reponame:RGO - Revista Gaúcha de Odontologia (Online)instname:Faculdade São Leopoldo Mandic (FSLM)instacron:FSLM10.1590/1981-863720180001000153289info:eu-repo/semantics/openAccessFRIEDRICH,Stephanie AnagnostopoulosRODRIGUES,JonasSILVA,Berenice Barbachan eeng2019-08-06T00:00:00Zoai:scielo:S1981-86372018000100106Revistahttp://revodonto.bvsalud.org/scielo.php?script=sci_serial&pid=1981-8637&lng=pt&nrm=isohttps://old.scielo.br/oai/scielo-oai.php||contato@revistargo.com.br1981-86370103-6971opendoar:2019-08-06T00:00RGO - Revista Gaúcha de Odontologia (Online) - Faculdade São Leopoldo Mandic (FSLM)false |
dc.title.none.fl_str_mv |
Albright hereditary osteodystrophy: dental management case report |
title |
Albright hereditary osteodystrophy: dental management case report |
spellingShingle |
Albright hereditary osteodystrophy: dental management case report FRIEDRICH,Stephanie Anagnostopoulos Dental care Oral manifestations Pseudohypoparathyroidism. |
title_short |
Albright hereditary osteodystrophy: dental management case report |
title_full |
Albright hereditary osteodystrophy: dental management case report |
title_fullStr |
Albright hereditary osteodystrophy: dental management case report |
title_full_unstemmed |
Albright hereditary osteodystrophy: dental management case report |
title_sort |
Albright hereditary osteodystrophy: dental management case report |
author |
FRIEDRICH,Stephanie Anagnostopoulos |
author_facet |
FRIEDRICH,Stephanie Anagnostopoulos RODRIGUES,Jonas SILVA,Berenice Barbachan e |
author_role |
author |
author2 |
RODRIGUES,Jonas SILVA,Berenice Barbachan e |
author2_role |
author author |
dc.contributor.author.fl_str_mv |
FRIEDRICH,Stephanie Anagnostopoulos RODRIGUES,Jonas SILVA,Berenice Barbachan e |
dc.subject.por.fl_str_mv |
Dental care Oral manifestations Pseudohypoparathyroidism. |
topic |
Dental care Oral manifestations Pseudohypoparathyroidism. |
description |
ABSTRACT Albright hereditary osteodystrophy is a disorder comprising phenotypic characteristics of genetic origin, such as short stature, obesity, and brachydactyly. It is a rare disorder and is related to pseudohypoparathyroidism. Within dentistry, it may be associated with enamel hypoplasia and late eruption. Furthermore, due to neurological problems, these patients may impose behavioural difficulties during dental appointments. The present study aims to describe the case of a patient with a possible diagnosis of Albright hereditary osteodystrophy, presenting symptoms and limitations to dental management. |
publishDate |
2018 |
dc.date.none.fl_str_mv |
2018-01-01 |
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=S1981-86372018000100106 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1981-86372018000100106 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.1590/1981-863720180001000153289 |
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 São Leopoldo Mandic |
publisher.none.fl_str_mv |
Faculdade São Leopoldo Mandic |
dc.source.none.fl_str_mv |
RGO - Revista Gaúcha de Odontologia v.66 n.1 2018 reponame:RGO - Revista Gaúcha de Odontologia (Online) instname:Faculdade São Leopoldo Mandic (FSLM) instacron:FSLM |
instname_str |
Faculdade São Leopoldo Mandic (FSLM) |
instacron_str |
FSLM |
institution |
FSLM |
reponame_str |
RGO - Revista Gaúcha de Odontologia (Online) |
collection |
RGO - Revista Gaúcha de Odontologia (Online) |
repository.name.fl_str_mv |
RGO - Revista Gaúcha de Odontologia (Online) - Faculdade São Leopoldo Mandic (FSLM) |
repository.mail.fl_str_mv |
||contato@revistargo.com.br |
_version_ |
1754204121999605760 |