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Updated: Jul 13, 2026

Creating Rigidly Stabilized Fractures for Assessing Intramembranous Ossification, Distraction Osteogenesis, or Healing of Critical Sized Defects
Published on: April 11, 2012
[Fibrodysplasia ossificans progressiva: case report]
Mariusz Puszczewicz1, Aleksandra Kołczewska, Irena Zimmermann-Górska
1Katedra i Klinika Reumatologiczno-Rehabilitacyjna i Chorób Wewnetrznych, Uniwersytet Medyczny im. Karola Marcinkowskiego, Pozna6i. puszczewicz@hotmail.com
Abstract:
Fibrodysplasia ossificans progressiva (FOP) is a rare genetic disease characterized by widespread soft tissue ossification and congenital stigmata of the extremities. We report the case of a 33-year-old woman with clinical and radiological features of FOP. She was born with bilateral hallux valgus and at the age of 10 presented swelling and ossification of the left scapula. During the course of the disease numerous crises were observed. In this patient authors noticed FOP exacerbation after a surgical operation.
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