A Case of Laurence-Moon-Biedl Syndrome
Journal of the Korean Ophthalmological Society
;
: 85-88, 1975.
Artículo
en Coreano
| WPRIM
| ID: wpr-130720
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:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Degeneración Retiniana
/
Agudeza Visual
/
Campos Visuales
/
Ceguera Nocturna
/
Polidactilia
/
Síndrome de Laurence-Moon
/
Degeneración Macular
/
Discapacidad Intelectual
/
Obesidad
Límite:
Adolescente
/
Humanos
/
Masculino
Idioma:
Coreano
Revista:
Journal of the Korean Ophthalmological Society
Año:
1975
Tipo del documento:
Artículo
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