透過您的圖書館登入
IP:3.136.17.118
  • 期刊

A Rare Case Report--Fibrodysplasia Ossificans Progressiva

罕見病例報告一進行性骨化性肌炎

並列摘要


Fibrodysplasia Ossificans Progressiva (FOP) is a rare congenital disease with autosomal transmission, characterized by the presence of malformations of great toes and of postnatal progressive heterotopic endochondral osteogenesis. We report a case of a three-year-old girl with dysplasia of the first metatarsal bones and progressive heterotopic ossificans on the right thigh after diphtheriatetanus- pertussis immunizations. The ossification progressed even after two surgical interventions, and resulted in progression of the disabilities of the right hip and right knee.

延伸閱讀