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An Unusual Case of Encephalomyeloradiculoneuropathy in a Young Woman
John S. Wendt, MD;
Jack S. Burks, MD
Arch Neurol. 1981;38(11):726-727.
Abstract
Fulminant and progressive CNS disease developed in a young woman and was associated with bilateral deafness and sharply elevated CSF protein levels. Two months after onset, a severe sensorimotor neuropathy developed. Clinical improvement occurred with corticosteroid therapy.
Author Affiliations
From the Rocky Mountain Multiple Sclerosis Center, University of Colorado Health Sciences Center, Denver. Dr Wendt is now with the Veterans Administration Medical Center, Dallas.
Footnotes
Accepted for publication March 8, 1981.
Reprint requests to Rocky Mountain Multiple Sclerosis Center, Box B-181, University of Colorado Health Sciences Center, 4200 E Ninth Ave, Denver, CO 80262 (Dr Wendt).
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