A Case of Laurence-Moon-Biedl Syndrome
Journal of the Korean Ophthalmological Society
;
: 85-88, 1975.
Artigo
em Coreano
| WPRIM
| ID: wpr-130725
ABSTRACT
A case of Laurence-Moon-Biedl Syndrome in 13-year-old Korean boy was reported with some clinical observation. Visual disturbance and night blindness were his chief complaints for about 3 years prior to visit our hospital. Visual acuity was 0.4 (O.S.,N.C.), 0.15 (O.D.,N.C.) and peripheral visual field was concentrically constricted with 30 degrees (0.5.), 15 degrees (O.D.). He had the atypical pigmentary retinal degeneration (O.D.) associated with obesity, polydactyly, mental retardation, hypogenitalism and macular degeneration (O.D.), but coudn't found the hereditary occurrence.
Texto completo:
DisponíveL
Índice:
WPRIM (Pacífico Ocidental)
Assunto principal:
Degeneração Retiniana
/
Acuidade Visual
/
Campos Visuais
/
Cegueira Noturna
/
Polidactilia
/
Síndrome de Laurence-Moon
/
Degeneração Macular
/
Deficiência Intelectual
/
Obesidade
Limite:
Adolescente
/
Humanos
/
Masculino
Idioma:
Coreano
Revista:
Journal of the Korean Ophthalmological Society
Ano de publicação:
1975
Tipo de documento:
Artigo
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