Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 1 de 1
Filter
Add filters








Language
Year range
1.
Journal of the Korean Ophthalmological Society ; : 633-635, 1980.
Article in Korean | WPRIM | ID: wpr-25556

ABSTRACT

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.


Subject(s)
Child , Female , Humans , Atrophy , Congenital Abnormalities , Extremities , Femur , Optic Atrophy , Osteopetrosis , Rare Diseases , Skull
SELECTION OF CITATIONS
SEARCH DETAIL