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Journal of the Korean Ophthalmological Society ; : 633-635, 1980.
Artículo en Coreano | WPRIM | ID: wpr-25556

RESUMEN

The authors experienced a case of osteopetrosis with optic atrophies and nystagmoid movements, exceedingly rare disease, in 12 year-old girl for 5 years without fracture in long bone. On the X-ray studies: 1. The skull bone showed moderately increased osteosclerotic changes in base of the skull and narrowings in optic foramina. 2. The findings of the extremities showed flask shaped deformities and cortical thickness in both femurs. and transverse line and epiphyseal separations in mid-tibia.


Asunto(s)
Niño , Femenino , Humanos , Atrofia , Anomalías Congénitas , Extremidades , Fémur , Atrofia Óptica , Osteopetrosis , Enfermedades Raras , Cráneo
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