Myoclonus in adult Huntington's disease
CM Vogel, I Drury, LC Terry… - Annals of Neurology …, 1991 - Wiley Online Library
CM Vogel, I Drury, LC Terry, AB Young
Annals of Neurology: Official Journal of the American Neurological …, 1991•Wiley Online LibraryTwo 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 epilipsy, although neither man had seizures. The
myoclonus was controlled with valproic acid therapy.
myoclonus years after the first signs of the disease. Their electroencephalograms were
consistent with a primary generalized epilipsy, although neither man had seizures. The
myoclonus was controlled with valproic acid therapy.
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 epilipsy, although neither man had seizures. The myoclonus was controlled with valproic acid therapy.