Hereditary form of sustained muscle activity of peripheral nerve origin causing generalized myokymia and muscle stiffness
- 1 January 1984
- journal article
- research article
- Published by Wiley in Annals of Neurology
- Vol. 15 (1) , 13-21
- https://doi.org/10.1002/ana.410150104
Abstract
Six patients in two unrelated families had a hereditary form of sustained muscle activity of peripheral nerve origin. Although varying in severity among affected family members, the disease was manifested clinically as generalized myokymia and muscle stiffness. Motor and sensory nerve conduction velocities and results of nerve biopsy were normal. Repetitive after‐discharges followed each motor nerve stimulus. Needle electrode examination demonstrated spontaneous recurrent bursts of motor unit activity. The burst activity of a motor unit occurred rhythmically (0.5 to 4 bursts per second) and independently of the activity of other units. Within a burst, the firing rate was high (150 to 300 Hz). The clinical and electromyographic abnormalities improved considerably after treatment with carbamazepine or phenytoin.This publication has 47 references indexed in Scilit:
- A dominantly inherited syndrome with continuous motor neuron dischargesAnnals of Neurology, 1983
- Limb myokymiaMuscle & Nerve, 1981
- Repetitive impulse‐induced emg discharges in neuromuscular diseasesAnnals of Neurology, 1981
- Neurotonia: Impulse‐induced repetitive discharges in motor nerves in peripheral neuropathyAnnals of Neurology, 1980
- Introduction of automated systems to evaluate touch‐pressure, vibration, and thermal cutaneous sensation in manAnnals of Neurology, 1978
- Hereditary persistent distal crampsJournal of Neurology, Neurosurgery & Psychiatry, 1972
- MYOKYMIA WITH IMPAIRED MUSCULAR RELAXATIONThe Lancet, 1969
- NeuromyotonieKlinische Wochenschrift, 1965
- GENERALISED MYOKYMIA IN THYROTOXICOSIS REPORT OF A CASEThe Lancet, 1954
- BeitrÄge zur MuskelpathologieZeitschrift für Neurologie, 1894