osteogenesis imperfecta

study design. we report 2 cases of acute cervical compression fracture in patients with osteogenesis imperfecta (oi).

研究设计：我们报告2例成骨不全（OI）患者急性颈椎压缩性骨折。

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after diagnosis, she was suffering from the rare "typical osteogenesis imperfecta" , which is the first in the southwest fairly.

经诊断，她患上的是罕见的“典型成骨不全症”，这在西南地区还算是首例。

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methods to review the effect of intravenous pamidronate therapy on two patients with osteogenesis imperfecta in 2007.

方法对2007年我院收治的2例成骨不全症的治疗进行回顾分析。

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Osteogenesis imperfecta ( OMIM 166200) is an autosomal dominant disorder characterized by bone fragility and abnormalities of connective tissue.

成骨不全病（OMIM166200）是一种常染色体显性遗传病，其临床表现以骨折及结缔组织异常为特征。

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Purpose To investigate the main points of diagnosing hereditary osteogenesis imperfecta.

目的探讨遗传性成骨不全诊断要点.

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objective to evaluate the diagnostic value of x-ray in osteogenesis imperfecta of fetus.

目的评估X线对胎儿期成骨不全的诊断价值。

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osteogenesis imperfecta (oi) is an inherited disease where basic pathology is of defective maturation of collagen.

成骨不全症（着）是一种遗传性疾病的基本病理是在有缺陷的成熟的胶原质。

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objective to summarize the experience of pamidronate for osteogenesis imperfecta.

目的总结帕米膦酸钠在成骨不全症中的应用经验。

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Objective To discuss the X-ray appearances of osteogenesis imperfecta.

目的探讨成骨不全症的 X 线诊断.

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osteogenesis imperfecta is an inherited disorder of connective tissue, which affects the skeleton, ligament, skin, sclera, and dentin.

骨发生不全是一种遗传性的结缔组织病变，常侵犯骨骼、韧带、皮肤、角膜及牙齿。

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