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[Myositis ossificans progressiva].

Revista medica hondurena, 2003
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Fibrodysplasia (Myositis) ossificans progressiva

Seminars in Arthritis and Rheumatism, 1994
Fibrodysplasia ossificans progressiva (FOP) is a rare hereditary connective tissue disorder. Patients with FOP develop progressive ossification of muscle and connective tissue associated with pain and disability. Onset is typically in childhood, and congenital anomalies of the feet are an early sign of this condition. Pain and stiffness of the spine or
Jh Miles, Amolak Singh, Alan J Bridges
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Myositis ossificans progressiva

Indian Journal of Pediatrics, 1958
1. Two cases of myositis ossificans progressiva are reported. 2. A brief review of the literature is presented.
O P Ghai
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Myositis Ossificans Progressiva

Journal of the Royal Society of Medicine, 1984
The case of a 19-year-old female patient with myositis ossificans progressiva is reported. This disease is a rare hereditary disorder with a dominant autosomal genotype. The patient had typical ossifications of the humeral and dorsal muscles, as well as of those of the left thigh and upper arm, and also an ankylosis of the left hip.
P, Pitt, E B, Hamilton
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MYOSITIS OSSIFICANS PROGRESSIVA

Pediatrics, 1951
Four new cases of myositis ossificans progressiva have been presented and the literature on the subject has been reviewed. At the onset typical cases will usually develop palpable masses over the fascial planes of the head and neck.
H D, RILEY, A, CHRISTIE
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