A Case of Type 1 Ushers Syndrome with Bilateral Cataract
Journal of the Korean Ophthalmological Society
; : 784-789, 1998.
Artigo
em Coreano
| WPRIM (Pacífico Ocidental)
| ID: wpr-226161
Biblioteca responsável:
WPRO
ABSTRACT
Ushers syndrome is an autosomal recessively inherited entity which is characterized by a retinitis pigmentosa and congenital sensorineural hearing loss. This syndrome represents different clinical features according to its subtypes. We experienced one case of type 1 Ushers syndrome, who had congenital hearing loss, visual field loss, visual loss of early childhood onset. We performed bilateral cataract extraction. Fundus examination after operation showed characteristic findings of retinitis pigmentosa. ERG was non-recordable ERG. Her audiogram confirmed the bilateral sensorineural hearing loss.
Texto completo:
Disponível
Base de dados:
WPRIM (Pacífico Ocidental)
Assunto principal:
Catarata
/
Extração de Catarata
/
Campos Visuais
/
Retinose Pigmentar
/
Síndromes de Usher
/
Perda Auditiva
/
Perda Auditiva Neurossensorial
Idioma:
Coreano
Revista:
Journal of the Korean Ophthalmological Society
Ano de publicação:
1998
Tipo de documento:
Artigo