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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
Alan J Bridges, Amolak Singh, Judith Miles   +2 more
exaly   +3 more sources

MYOSITIS OSSIFICANS PROGRESSIVA

Journal of Bone and Joint Surgery: British Volume, 1954
In 1692 Patin (1) described the first case of progressive muscle ossification and in 1868 von Dusch (2) gave the disease its present name of myositis ossificans progressiva. A detailed survey of the literature was published by Rosenstirn (3) in 1918, and in 1932 Mair (4) reviewed the subject thoroughly and published two cases of his own.
F Harwood Stevenson
exaly   +3 more sources

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, B N, SINGH, D P, MUKERJEA
exaly   +3 more sources

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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