Congenital Aniridia in a Family for Three Generations
Journal of the Korean Ophthalmological Society
;
: 383-389, 1990.
Artículo
en Coreano
| WPRIM
| ID: wpr-222147
ABSTRACT
Aniridia is a congenital, often hereditary, usually bilateral absence of iris in whole or in part. And aniridia occurs mainly as an autosomal dominant condition with almost complete penetrance. In the usual phenotype, aniridia is associated with nystagmus, foveal and optic nerve hypoplasia, corneal pannus, cataract, secondary glaucoma and strabismus. The author experienced 4 cases of aniridia in a family for three generations. So the author reports these cases with the review of literathure.
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Nervio Óptico
/
Fenotipo
/
Aniridia
/
Glaucoma
/
Composición Familiar
/
Iris
/
Estrabismo
/
Penetrancia
/
Opacificación Capsular
Límite:
Humanos
Idioma:
Coreano
Revista:
Journal of the Korean Ophthalmological Society
Año:
1990
Tipo del documento:
Artículo
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