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Japanese

Myoclonus epilepsy with brown pigment and cerebellar cortical degeneration. Shigeki TAKEDA 1 , Hitoshi TAKAHASHI 1 , Eisaku OHAMA 1 , Fusahiro IKUTA 1 , Haruhiko NAITO 2 , Tadashi ARITA 2 1Department of Experimental Neuropathology, Brain Research Institute, Niigata University 2Department of Psychiatry, School of Medicine, Niigata University pp.142-152
Published Date 1987/2/10
DOI https://doi.org/10.11477/mf.1431905871
  • Abstract
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 We report the postmortem findings of a 28-year-old housewife who was clinically diagnosed as having progressive myoclonus epilepsy and pathologically had the characteristic extraneuronal pigments and the degeneration of the cerebellar cortex as well as of the dentatorublar and pallidoluysian systems.

 There is no family history of neurological and psychiatric diseases. At age 20, she developed asthenic attack of extremities and cerebellar ataxia. Ten months later, epilepsy was suggested by EEG finding and daily administration of diphenylhydantoin (DPH, 200 mg/day) and other antiepileptic drugs was started.


Copyright © 1987, Igaku-Shoin Ltd. All rights reserved.

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電子版ISSN 1882-1243 印刷版ISSN 0001-8724 医学書院

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