Early-onset autosomal dominant retinitis pigmentosa with severe hyperopia.
Am J Ophthalmol
; 111(4): 454-6, 1991 Apr 15.
Article
en En
| MEDLINE
| ID: mdl-2012147
ABSTRACT
We studied a four-generation family with early-onset autosomal dominant retinitis pigmentosa, severe hyperopia, and axial eye lengths of less than 20 mm. The affected members had decreased vision, night blindness, typical peripheral retinal pigmentary changes, and electroretinographic abnormalities characteristic of retinitis pigmentosa. This pedigree suggests there is another variant of retinitis pigmentosa associated with hyperopia besides Leber's congenital amaurosis and preserved para-arteriole retinal pigment epithelium.
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Base de datos:
MEDLINE
Asunto principal:
Retinitis Pigmentosa
/
Hiperopía
Tipo de estudio:
Etiology_studies
Límite:
Adolescent
/
Adult
/
Aged
/
Child
/
Female
/
Humans
/
Male
/
Middle aged
Idioma:
En
Revista:
Am J Ophthalmol
Año:
1991
Tipo del documento:
Article