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Activation of Fibrinolysis in Muscular Dystrophy
Peter H. Berman, MD;
Michael A. Nigro, DO;
Michael B. Harris, MD;
Frank A. Oski, MD
Arch Neurol. 1973;29(1):65-66.
Abstract
Ten of 16 boys with Duchenne muscular dystrophy and one of 11 patients with limbgirdle muscular dystrophy were found to have increased content of fibrin split products in serum. In both diseases, an increase in the content of fibrin split products was found only in those patients in whom the creatine phosphokinase activity was greater than 1,000 international units, suggesting that the activation of fibrinolysis in muscular dystrophy results from leakage of plasminogen-activator from diseased muscle.
Author Affiliations
Philadelphia
From the departments of neurology (Drs. Berman and Nigro) and pediatrics (Drs. Berman, Harris and Oski), University of Pennsylvania and the divisions of neurology and hematology, the Children's Hospital of Philadelphia.
Footnotes
Accepted for publication March 30, 1973.
Reprint requests to the Division of Neurology, Children's Hospital of Philadelphia, 1740 Bainbridge St, Philadelphia (Dr. Berman).
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