J Korean Acad Rehabil Med.  1997 Dec;21(6):1249-1253.

Myositis Ossificans Progressiva: A Case Report

Affiliations
  • 1Department of Rehabilitation Medicine, Dongguk University College of Medicine, Korea.

Abstract

Myositis ossificans progressiva, a rare autosomal dominant disorder, is characterized by progressive heterotopic ossification of muscle and connective tissue associated with pain and disability. I have experienced a 15-year-old woman with multiple contracture and deformity in both lower extremities. Clinical features and laboratory findings including electrodiagnostic findings were compatible with myositis ossificans progressiva. I report this case with the review of literature.

Keyword

Myositis ossificans progressiva; Electrodiagnostic findings

MeSH Terms

Adolescent
Congenital Abnormalities
Connective Tissue
Contracture
Female
Humans
Lower Extremity
Myositis Ossificans*
Myositis*
Ossification, Heterotopic
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