Suzuki S, Kamoshita S, Ninomura S
Department of Pediatrics, Jichi Medical School, Tochigi, Japan.
Pediatr Neurol. 1985 Sep-Oct;1(5):298-301. doi: 10.1016/0887-8994(85)90032-3.
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.