Bilateral Complicated Microphthalmia in a Family
Journal of the Korean Ophthalmological Society
; : 1031-1035, 1989.
Article
em Ko
| WPRIM
| ID: wpr-194110
Biblioteca responsável:
WPRO
ABSTRACT
Complicated microphthalmos can be diagnosed when a reduction in global dimension is combined with other structural anomalies. These include corneal opacity or staphyloma, cataract, aniridia, corectopia, persistence of pupillary membrane or the tunica vasculosa lentis and hyaloid vessel, thickening or ossification of the choroid and various retinal anomalies. Complicated microphthalmos is frequently hereditary and the transmission may be either as an autosomal dominant or recessive or as a sex linked recessive trait. Four cases of bilateral complicated microphthalmos with cataract were found in a family.
Palavras-chave
Texto completo:
1
Índice:
WPRIM
Assunto principal:
Retinaldeído
/
Catarata
/
Aniridia
/
Microftalmia
/
Corioide
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Opacidade da Córnea
/
Membranas
Limite:
Humans
Idioma:
Ko
Revista:
Journal of the Korean Ophthalmological Society
Ano de publicação:
1989
Tipo de documento:
Article