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KMID : 0358419750180060421
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Korean Journal of Obstetrics and Gynecology
1975 Volume.18 No. 6 p.421 ~ p.426
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A Case of Osteogenesis Iinperfecta
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Abstract
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Osteogenesis imperfecta is a rare inherited condition in which the bones are abnormally brittle and easily fractured. The disease begins in fetal life, but rarely become manifest , before infancy or early childhood.
The basic pathology is hypoplasia of the mesenchyme. The disease is a complex one with numerous systemic manifestations and classifications.
Authors reports a case of osteogenesis imperfecta congenita with brief review of literatures.
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