Hirayama disease with juvenile myoclonic epilepsy: A case report

Jin Sung Park, Sung Pa Park, Jong Geun Seo

Research output: Contribution to journalArticlepeer-review

2 Scopus citations

Abstract

Hirayama disease (HD) is rare, but benign anterior horn cell disease, predominantly affecting young men. One of the symptoms, besides weakness, is abnormal movement in the hand. Juvenile myoclonic epilepsy (JME) is one of the most common types of generalized epilepsies and can be recognized by a myoclonic jerk and electroencephalography (EEG) features. We report the case of a 19-year-old male who had HD, with unilateral abnormal movement in the hand, which was diagnosed as JME. We should consider performing an EEG in patients with HD, who present with atypical hand movements, in order to differentiate it from seizure.

Original languageEnglish
Pages (from-to)358-360
Number of pages3
JournalAnnals of Indian Academy of Neurology
Volume17
Issue number3
DOIs
StatePublished - 2014

Keywords

  • Electroencephalography
  • Hirayama disease
  • juvenile myoclonic epilepsy
  • myoclonus

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