【摘 要】
：
Fibrodysplasia ossificans progressiva (FOP) that caused by mutation in the ACVR1 gene is an autosomal dominant disorder of the musculoskeletal disease characterized by progressive disability due to he
【机 构】
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Department of Neurology, Peking University First Hospital
【出 处】
：
The 12th Annual Asian and Oceanian Myology Center (AOMC)Scie
论文部分内容阅读
Fibrodysplasia ossificans progressiva (FOP) that caused by mutation in the ACVR1 gene is an autosomal dominant disorder of the musculoskeletal disease characterized by progressive disability due to heterotopic ossification of skeletal muscles and restriction of joints rendering body movements impossible.There is no known effective therapy for FOP.To report the effect of corticosteroids and warfarin in FOP.
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