Publicação

Ophthalmology case

Ver documento

Detalhes bibliográficos
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.
Autores principais:Fernandes,Alexandra
Outros Autores:Madureira,Cristina; Pinto,Fátima
Assunto:Brown syndrome ocular motility disorder restriction of elevation in adduction
Ano:2018
País:Portugal
Tipo de documento:relatório
Tipo de acesso:acesso aberto
Instituição associada:Fundação para a Ciência e Tecnologia
Idioma:inglês
Origem:SciELO Portugal
Descrição
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.