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KMID : 0377619740260060716
Korean Jungang Medical Journal
1974 Volume.26 No. 6 p.716 ~ p.718
A Case Report of Osteogenesis Imperfecta


Abstract
A case report of Osteogenesis imperfecta, of which the incidence is not common, and the disease is a generalized disorder of the connective tissue.
The disease, clinically, is characterized by fragile bones, with or without the blue sclera and deafness, and inherited as autosomal dominant.
There is no familial history in this case.
One case of Osteogenesis imperfecta in 6 years old Korean female, which is experienced by the author recently, is reported.
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