Visual function in Laurence-Moon-Bardet-Biedl syndrome. A survey of 26 cases.
Acta Ophthalmol Suppl (1985)
; 182: 128-31, 1987.
Article
em En
| MEDLINE
| ID: mdl-2837047
ABSTRACT
In 1984, 32 persons with Laurence-Moon-Bardet-Biedl syndrome (LMBB syndrome) were registered in Norway. Of these, 26 stayed for 10 days at the Frambu Health Centre, where they consulted a pediatrician, a psychologist, a dentist, a social worker, a geneticist, a teacher for the blind and an ophthalmologist. The ocular examination showed the eye disease in cases of LMBB syndrome to be homogeneous and fulminant tapetoretinal degeneration of the retinitis pigmentosa type.
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Base de dados:
MEDLINE
Assunto principal:
Visão Ocular
/
Síndrome de Laurence-Moon
Limite:
Adolescent
/
Adult
/
Child
/
Child, preschool
/
Female
/
Humans
/
Male
/
Middle aged
Idioma:
En
Revista:
Acta Ophthalmol Suppl (1985)
Ano de publicação:
1987
Tipo de documento:
Article
País de afiliação:
Noruega