Open-Biopsy Electromyography
- 1 July 1979
- journal article
- research article
- Published by American Medical Association (AMA) in Archives of Neurology
- Vol. 36 (7) , 406-409
- https://doi.org/10.1001/archneur.1979.00500430036004
Abstract
• Open-biopsy electromyography (EMG) of two muscles of a 29-year-old man with slowly progressive proximal weakness demonstrated a striking pattern of excessively recruited, pathologically small motor unit potentials. This pattern is usually equated with myopathy. Histologic study of tissue enclosing the recording sites, however, yielded evidence of neurogenic disease alone. In muscle, this included isolated and small groups of atrophic type I, IIA, and IIB fibers, and in intramuscular nerve a loss of myelinated fibers with connective tissue and Schwann cell proliferation. The EMG pattern is considered to reflect a reduced number of activated muscle fibers within motor units due to random neurogenic involvement of terminal axons.This publication has 3 references indexed in Scilit:
- The baseline, the time characteristics and the slow afterwaves of the motor unit potentialElectroencephalography and Clinical Neurophysiology, 1973
- Histological and histochemical changes in skeletal muscle from cases of chronic juvenile and early adult spinal muscular atrophy (the Kugelberg-Welander syndrome)Journal of the Neurological Sciences, 1971
- Myopathic electromyographic changes correlated with histopathology in Wohlfart‐Kugelberg‐Welander diseaseNeurology, 1969