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A severely disabling disorder: fibrodysplasia ossificans progressiva.

作者信息

Kocyigit H, Hizli N, Memis A, Sabah D, Memis A

机构信息

Izmir Atatürk Training Hospital, Turkey.

出版信息

Clin Rheumatol. 2001;20(4):273-5. doi: 10.1007/s100670170044.

Abstract

Fibrodysplasia ossificans progressiva (FOP) is an extremely rare hereditary disorder characterised by progressive heterotopic ossification of the soft tissues. The resulting progressive immobilisation of the limbs, jaw and chest wall generally leads to severe disability. We present an 18-year-old girl with advanced FOP. She had three operative interventions to excise her ectopic bones but all resulted in failure. Treatment strategies for this disorder should include the avoidance of exacerbating factors.

摘要

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