Systematic Affection of Bone in the Department of Orthopedic Surgery, Tottori University School of Medicine
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The authors described the clinical features, radiologic findings and laboratory findings in four patients-osteogenesis imperfecta congenita (thick bone type), osteogenesis imperfecta tarda without fracture, gargoylism and Albright's syndrome-out of 13 patients with the systematic affection of the bone were registered in the department of orthopedic surgery, Tottori university school of medicine, for the past six months.Especially, in a patient with Albright's syndrome, the laboratory examinations were performed in detail. As a consequence, the serum human growth hormone measured by radioimmunoassay was remarkedly elevated (124mμl/ml), Thereby, some etiologies of Albright's syndrome were discussed.
- 西日本整形・災害外科学会の論文
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