FIBRODYSPLASIA (MYOSITIS) OSSIFICANS PROGRESSIVA: TWO CASES REPORT
Sibel Özbudak Demir1, Göknur Karahan1, Gülümser Aydın2, Füsun Köseoğlu1
Keywords: Fibrodysplasia ossificans progressiva
Abstract
Fibrodysplasia (myositis) ossificans progresiva (FOP) is a hereditary mesodermal tissue characterized by progressive ossification of striated muscle, tendon, ligament, fasciae, aponeurose and occasionally skin. The pattern of inheritance remains unknown. Indeed, most reported cases are the result of spontaneous mutations. In this article we present two cases with FOP and reviewed the literature.