osteogenesis imperfecta

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。

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。

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。

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

目的探讨成骨不全症的 X 线诊断.

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。

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。

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。

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.

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。

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。