Ophthalmology case

Detalhes bibliográficos
Autor(a) principal: Fernandes,Alexandra
Data de Publicação: 2018
Outros Autores: Madureira,Cristina, Pinto,Fátima
Tipo de documento: Relatório
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://scielo.pt/scielo.php?script=sci_arttext&pid=S0872-07542018000300014
Resumo: Brown syndrome is a rare ocular motility abnormality characterized by a restriction of the superior oblique tendon, which results in a restriction of elevation in adduction. This entity can be congenital or acquired. The cause of congenital Brown`s syndrome remains unknown but some cases with a family history have been described. Spontaneous resolution occurs between 20 to 30%. We describe a case of an eight-year-old boy with congenital Brown syndrome.
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spelling Ophthalmology caseBrown syndromeocular motility disorderrestriction of elevation in adductionBrown syndrome is a rare ocular motility abnormality characterized by a restriction of the superior oblique tendon, which results in a restriction of elevation in adduction. This entity can be congenital or acquired. The cause of congenital Brown`s syndrome remains unknown but some cases with a family history have been described. Spontaneous resolution occurs between 20 to 30%. We describe a case of an eight-year-old boy with congenital Brown syndrome.Centro Hospitalar do Porto2018-09-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/reporttext/htmlhttp://scielo.pt/scielo.php?script=sci_arttext&pid=S0872-07542018000300014Nascer e Crescer v.27 n.3 2018reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAPenghttp://scielo.pt/scielo.php?script=sci_arttext&pid=S0872-07542018000300014Fernandes,AlexandraMadureira,CristinaPinto,Fátimainfo:eu-repo/semantics/openAccess2024-02-06T17:06:20Zoai:scielo:S0872-07542018000300014Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-20T02:19:45.302747Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Ophthalmology case
title Ophthalmology case
spellingShingle Ophthalmology case
Fernandes,Alexandra
Brown syndrome
ocular motility disorder
restriction of elevation in adduction
title_short Ophthalmology case
title_full Ophthalmology case
title_fullStr Ophthalmology case
title_full_unstemmed Ophthalmology case
title_sort Ophthalmology case
author Fernandes,Alexandra
author_facet Fernandes,Alexandra
Madureira,Cristina
Pinto,Fátima
author_role author
author2 Madureira,Cristina
Pinto,Fátima
author2_role author
author
dc.contributor.author.fl_str_mv Fernandes,Alexandra
Madureira,Cristina
Pinto,Fátima
dc.subject.por.fl_str_mv Brown syndrome
ocular motility disorder
restriction of elevation in adduction
topic Brown syndrome
ocular motility disorder
restriction of elevation in adduction
description Brown syndrome is a rare ocular motility abnormality characterized by a restriction of the superior oblique tendon, which results in a restriction of elevation in adduction. This entity can be congenital or acquired. The cause of congenital Brown`s syndrome remains unknown but some cases with a family history have been described. Spontaneous resolution occurs between 20 to 30%. We describe a case of an eight-year-old boy with congenital Brown syndrome.
publishDate 2018
dc.date.none.fl_str_mv 2018-09-01
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/report
format report
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://scielo.pt/scielo.php?script=sci_arttext&pid=S0872-07542018000300014
url http://scielo.pt/scielo.php?script=sci_arttext&pid=S0872-07542018000300014
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv http://scielo.pt/scielo.php?script=sci_arttext&pid=S0872-07542018000300014
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 Centro Hospitalar do Porto
publisher.none.fl_str_mv Centro Hospitalar do Porto
dc.source.none.fl_str_mv Nascer e Crescer v.27 n.3 2018
reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron:RCAAP
instname_str Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron_str RCAAP
institution RCAAP
reponame_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
collection Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository.name.fl_str_mv Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
repository.mail.fl_str_mv
_version_ 1817553721768280064

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