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A Case of Osteopetrosis with Optic Atrophy
Article 在 Ko | WPRIM | ID: wpr-25556
Responsible library: WPRO
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)
全文: 1 索引: WPRIM 主要主题: Osteopetrosis / Atrophy / Skull / Congenital Abnormalities / Optic Atrophy / Rare Diseases / Extremities / Femur 限制: Child / Female / Humans 语言: Ko 期刊: Journal of the Korean Ophthalmological Society 年: 1980 类型: Article
全文: 1 索引: WPRIM 主要主题: Osteopetrosis / Atrophy / Skull / Congenital Abnormalities / Optic Atrophy / Rare Diseases / Extremities / Femur 限制: Child / Female / Humans 语言: Ko 期刊: Journal of the Korean Ophthalmological Society 年: 1980 类型: Article