Papillo-renal syndrome. An inherited association of optic disc dysplasia and renal disease. Report and review of the literature.
Ophthalmic Paediatr Genet
; 10(3): 185-98, 1989 Sep.
Article
en En
| MEDLINE
| ID: mdl-2685703
ABSTRACT
A family is described in which the father and son had chronic renal disease of early onset and bilateral optic nerve dysplasia. A further son, known to have microphthalmos died of renal disease in childhood. Optic nerve changes included coloboma in the father and Handmann's optic nerve anomaly, a condition resembling the morning glory syndrome (M.G.S.), in the son. There was electrodiagnostic and visual field evidence of optic nerve dysfunction even where acuity was relatively unaffected. The son developed central serous retinopathy, a condition frequently encountered in association with optic nerve dysplasias, including M.G.S.
Buscar en Google
Colección:
01-internacional
Banco de datos:
MEDLINE
Asunto principal:
Enfermedades del Nervio Óptico
/
Fallo Renal Crónico
Tipo de estudio:
Risk_factors_studies
Límite:
Adult
/
Aged
/
Aged80
/
Child
/
Humans
/
Male
/
Middle aged
Idioma:
En
Revista:
Ophthalmic Paediatr Genet
Año:
1989
Tipo del documento:
Article
País de afiliación:
Reino Unido