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A. Gruca (1925)
MYOSITIS OSSIFICANS CIRCUMSCRIPTA: A CLINICAL AND EXPERIMENTAL STUDYAnnals of Surgery, 82
W. Bauer, A. Marble, G. Bennett (1931)
FURTHER STUDIES IN A CASE OF CALCIFICATION OF SUBCUTANEOUS TISSUE (“CALCINOSIS UNIVERSALIS”) IN A CHILDThe American Journal of the Medical Sciences, 713
William Mair (1932)
Myositis Ossificans ProgressivaEdinburgh Medical Journal, 39
W. Wilkins, E. Regen, G. Carpenter (1935)
PHOSPHATASE STUDIES ON BIOPSY TISSUE IN PROGRESSIVE MYOSITIS OSSIFICANS: WITH A REPORT OF A CASEJAMA Pediatrics, 49
J. Mather (1931)
Progressive Myositis OssificansBritish Journal of Radiology, 4
B. Frejka
HETEROTOPIC OSSIFICATION AND MYOSITIS OSSIFICANS PROGRESSIVAJournal of Bone and Joint Surgery, American Volume, 11
R. Maudsley (1952)
Case of Myositis Ossificans ProgressivaBritish Medical Journal, 1
S. Creveld, J. Soeters (1941)
MYOSITIS OSSIFICANS PROGRESSIVAJAMA Pediatrics, 62
H. Riley, Amos Christie (1951)
Myositis ossificans progressiva.Pediatrics, 8 6
J. Hartley, S. Tanz (1951)
Experimental osteogenesis in rabbit muscle.A.M.A. archives of surgery, 63 6
K. Ryan (1945)
Myositis ossificans progressivaThe Journal of Pediatrics, 27
Geschickter Cf, Copeland Mm (1951)
Classification of bone tumors.Bulletin of the Hospital for Joint Diseases, 12
Amos Koontz (1927)
MYOSITIS OSSIFICANS PROGRESSIVAThe American Journal of the Medical Sciences, 174
MYOSITIS ossificans progressiva is a rare disease characterized by the formation of areas of calcification in the interstitial connective tissue of muscles, tendons, ligaments, fascia, and aponeuroses. Although manifestations of the disease may not begin until after 10 years of age, certain associated congenital anomalies are ordinarily present at birth, especially microdactyly of the thumbs and big toes. There may be exacerbations and remissions of the disease, but the general course is an insidious loss of body motion, affecting especially the neck, spine, and upper extremities and, rarely, the hips and lower extremities. The masseters are sometimes so severely involved that chewing becomes difficult. The heart, diaphragm, tongue, larynx, and sphincters are spared. The following patient is a rather typical example of this interesting and dramatic clinical picture who was given corticotropin (ACTH) with probably slight improvement. The progressively immobilizing features in this child were, however, irreversible, and no known
American journal of diseases of children – American Medical Association
Published: May 1, 1954
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