Three Cases of Congenital Aniridia in One Family
Journal of the Korean Ophthalmological Society
;
: 282-287, 2000.
Artigo
em Coreano
| WPRIM
| ID: wpr-108427
ABSTRACT
Aniridia is a relatively rare congenital anomaly and its incidence is about 1100, 000.Main features of aniridia include congenitally partial or nearly complete absence of the iris and hypoplasia of optic disc and fovea. It is almost bilateral and occurred as an autosomal dominant trait.However, some patients develop both sporadic nonfamilial aniridia and Wilms 'tumor, and another group of patients is transmitted as an autosomal recessive trait. We observed aniridia in two generations, as mother and two daughters. They had cataract, nystagmus, neovascularization of corneal margin and pannus formation, as well as aniridia.We also found hypoplasia of optic disc and fovea in mother. We have operated on mother with phacoemulsified lens aspiration and posterior chamber IOL implantation in both eyes consecutively.The postoperative visual acuity following lens extraction improved, but was not corrected. In addition, intraocular pressure decreased.
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Assunto principal:
Catarata
/
Núcleo Familiar
/
Acuidade Visual
/
Aniridia
/
Características da Família
/
Iris
/
Incidência
/
Pressão Intraocular
/
Mães
Tipo de estudo:
Estudo de incidência
/
Estudo prognóstico
Limite:
Humanos
Idioma:
Coreano
Revista:
Journal of the Korean Ophthalmological Society
Ano de publicação:
2000
Tipo de documento:
Artigo
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