Myoclonus in adult Huntington's disease.

Vogel, C M; Drury, I; Terry, L C; Young, A B · Ann Neurol · 1991

case_report · Level V

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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.

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