Mobility challenges and solutions for fibrodysplasia ossificans progressiva.

Fibrodysplasia ossificans progressiva (FOP) is a rare genetic disorder characterized by progressive soft tissue ossification. Although signs may be present at birth, the first appearance of ectopic bone typically occurs in early childhood. The primary target is the axial musculature. Eventually ectopic bone also occurs in ligaments, fascia, aponeurosis, tendons, and joint capsules of the appendicular skeleton with a proximal to distal predilection. As the disease advances, mobility becomes restricted, and affected individuals are typically limited to bed or chair by their early 30s. This report describes a 30-year-old woman with advanced FOP. She had a fused spine and a fixed pelvis, with hips and knees locked in flexion and feet in plantarflexion. Her upper limb mobility was similarly restricted. She was not able to stand upright or sit independently. The modification of a commercially available power wheelchair that allowed the patient to maintain her employment as a preschool teacher and custom shoes are described. Creative physiatric intervention is essential to liberate human potential for people with FOP.

[1]  D. Wieder Treatment of traumatic myositis ossificans with acetic acid iontophoresis. , 1992, Physical therapy.

[2]  W. Kussmaul,et al.  Pulmonary and cardiac function in advanced fibrodysplasia ossificans progressiva. , 1998, Clinical orthopaedics and related research.

[3]  J. Giurini,et al.  In-Shoe Foot Pressure Measurements in Diabetic Patients With At-Risk Feet and in Healthy Subjects , 1994, Diabetes Care.

[4]  H. Skirton,et al.  A three generation family with fibrodysplasia ossificans progressiva. , 1993, Journal of medical genetics.

[5]  M. Muenke,et al.  Genetic transmission of fibrodysplasia ossificans progressiva. Report of a family. , 1993, The Journal of bone and joint surgery. American volume.

[6]  A. Boulton,et al.  The Association Between Callus Formation, High Pressures and Neuropathy in Diabetic Foot Ulceration , 1996, Diabetic medicine : a journal of the British Diabetic Association.

[7]  Olmedo Garzón Fj,et al.  Fibrodysplasia Ossificans Progressiva , 1984, Definitions.

[8]  M. Muenke,et al.  Overexpression of an osteogenic morphogen in fibrodysplasia ossificans progressiva. , 1996, The New England journal of medicine.

[9]  J. Connor,et al.  Genetic aspects of fibrodysplasia ossificans progressiva. , 1982, Journal of medical genetics.

[10]  A. Superti-Furga,et al.  Heritable Disorders of Connective Tissues , 1990 .

[11]  David M. Rocke,et al.  Age- and joint-specific risk of initial heterotopic ossification in patients who have fibrodysplasia ossificans progressiva. , 1994, Clinical orthopaedics and related research.