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KMID : 0371619860020010055
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Journal of Wonkwang Medical Science
1986 Volume.2 No. 1 p.55 ~ p.59
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A Case of Congenital Osteogenesis Imperfecta
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Abstract
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hat affects the skeleton, ligament, sclera and dentin.
We experienced a case of Group II osteogenesis imperfecta in a day old female patient.
This disease is characterized by spontaneous fracture of bone, otosclerosis, deafness and blue sciera.
Related liteOsteogenesis Imperfecta is a inherited disorder of connective tissue t-rature was briefly reviewed.
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KEYWORD
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FullTexts / Linksout information
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Listed journal information
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