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Myoclonus in adult Huntington's disease
C M Vogel1, I Drury, L C Terry
1Department of Neurology, University of Michigan Medical School, Ann Arbor.
Annals of Neurology
|February 1, 1991
Abstract:
Two brothers with clinically definite adult Huntington's disease developed disabling myoclonus years after the first signs of the disease. Their electroencephalograms were consistent with a primary generalized epilepsy, although neither man had seizures. The myoclonus was controlled with valproic acid therapy.