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Ramsay Hunt syndrome in dentatorubral-pallidoluysian atrophy
S Suzuki1, S Kamoshita, S Ninomura
1Department of Pediatrics, Jichi Medical School, Tochigi, Japan.
Pediatric Neurology
|September 1, 1985
Abstract:
We report a case of Ramsay Hunt syndrome which was clinically characterized by myoclonus epilepsy, cerebellar ataxia, convulsions, and dementia. Major necropsy findings were dentatorubral-pallidoluysian atrophy. Dentatorubral-pallidoluysian atrophy may be associated with a variety of clinical symptoms, amongst which Ramsay Hunt syndrome can be included.