Osteogenesis imperfecta

被引:13
|
作者
Forin, Veronique [1 ]
机构
[1] Hop Enfants Armand Trousseau, Unite Pediat Med Phys & Readaptat, F-75012 Paris, France
来源
PRESSE MEDICALE | 2007年 / 36卷 / 12期
关键词
D O I
10.1016/j.lpm.2007.01.043
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Osteogenesis imperfecta is a genetic disorder that causes increased bone fragility and low bone moss. Osteogenesis imperfecta is a rare disease: its estimated prevalence is between 1/10 000 and 1/20 000 persons. The severity of skeletal and extraskeletal manifestations varies widely. Most patients hove a mutation in one of the 2 genes that encode the alpha chains of collagen type I. Treatment with bisphosphonates has produced clear improvements, especially for growing children. The appropriate regimen for bisphosphonate treatment remains to be determined. the goal is to find the lowest effective dose to minimize side effects. Treatment of osteogenesis imperfecta must be multidisciplinary including physicians, surgeons, and physical therapists.
引用
收藏
页码:1787 / 1793
页数:7
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