A Case of Stickler`s Syndrome
Journal of the Korean Ophthalmological Society
;
: 2043-2047, 1999.
Artigo
em Coreano
| WPRIM
| ID: wpr-108598
ABSTRACT
Stickler`s syndrome is a progressive, connective tissue disease which has an autosomal dominant trait with variable penetrance. Ocular changes include vitreoretinal degenera- tion, retinal pigmentary changes, retinal detachment, chori- oretinal atrophy, cataract and high myopia. Systemically, characteristic facial appearances, musculoskeletal abnormal- ities and hearing loss may be associated. We experienced a sporadic case of Stickler`s syndrome in a neonate and report with a review of the literatures.
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Assunto principal:
Retinaldeído
/
Atrofia
/
Catarata
/
Descolamento Retiniano
/
Doenças do Tecido Conjuntivo
/
Penetrância
/
Perda Auditiva
/
Miopia
Limite:
Humanos
/
Recém-Nascido
Idioma:
Coreano
Revista:
Journal of the Korean Ophthalmological Society
Ano de publicação:
1999
Tipo de documento:
Artigo
Similares
MEDLINE
...
LILACS
LIS