Abstract:
:We studied the effect of a single oral intake of 30 to 40 grams of alcohol in 4 consecutive patients presenting with Ramsay Hunt syndrome, the most common type of degenerative progressive myoclonic epilepsy (PME) encountered in southern Europe. Clinical and polygraphic monitoring demonstrated abatement of myoclonus in all patients, although the degree of improvement varied among patients. These findings show that alcohol is a potent antimyoclonic agent. In the particular context of PME, occasional alcohol intake may help patients in their social life.
journal_name
Neurologyjournal_title
Neurologyauthors
Genton P,Guerrini Rdoi
10.1212/wnl.40.9.1412subject
Has Abstractpub_date
1990-09-01 00:00:00pages
1412-6issue
9eissn
0028-3878issn
1526-632Xjournal_volume
40pub_type
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