PROGRESSIVE NEUROPATHIC (PERONEAL) MUSCULAR ATROPHY (CHARCOT-MARIE-TOOTH DISEASE)
- 1 July 1953
- journal article
- other
- Published by American Medical Association (AMA) in A.M.A. Archives of Neurology & Psychiatry
- Vol. 70 (1) , 1-29
- https://doi.org/10.1001/archneurpsyc.1953.02320310007001
Abstract
THERE seems to be a general feeling among neurologists that one is justified in considering as a disease entity the condition variously called "peroneal muscular atrophy of the Charcot-Marie-Tooth type," "progressive neuritic muscular atrophy," or "spinal neuritic form of progressive muscular atrophy." The weight of available evidence concerning its etiology, most recently reviewed by England and Denny-Brown,1is in favor of an affection of the spinal cord and of peripheral nerves being the primary process, the muscular changes being secondary; but few autopsy reports are found in the literature. However, biopsy of affected muscles may give information of interest, since it is now well established that the histological changes in the muscles in progressive muscular dystrophies differ in certain respects from those occurring in diseases involving primarily the peripheral motor neurons, such as amytrophic lateral sclerosis, progressive spinal muscular atrophy, syringomyelia, and poliomyelitis.2Brodal and Refsum3describedKeywords
This publication has 1 reference indexed in Scilit:
- ELECTROMYOGRAPHY IN MUSCULAR DYSTROPHIES: DIFFERENTIATION BETWEEN DYSTROPHIES AND CHRONIC LOWER MOTOR NEURONE LESIONSJournal of Neurology, Neurosurgery & Psychiatry, 1949