MeSH 搜索器

Myoclonic Epilepsy, Juvenile

A disorder characterized by the onset of myoclonus in adolescence, a marked increase in the incidence of absence seizures (see EPILEPSY, ABSENCE), and generalized major motor seizures (see EPILEPSY, TONIC-CLONIC). The myoclonic episodes tend to occur shortly after awakening. Seizures tend to be aggravated by sleep deprivation and alcohol consumption. Hereditary and sporadic forms have been identified. (From Adams et al., Principles of Neurology, 6th ed, p323)
推出的年份: 2000
副标题
树号: C10.228.140.490.375.130.670, C10.228.140.490.493.063.670
MeSH 单一 ID: D020190
进入的组:
  • Epilepsy, Juvenile Myoclonic
  • Impulsive Petit Mal, Janz
  • Janz Syndrome
  • Juvenile Myoclonic Epilepsy
  • Impulsive Petit Mal Epilepsy
  • Janz Impulsive Petit Mal
  • Janz Juvenile Myoclonic Epilepsy
  • Juvenile Myoclonic Epilepsy of Janz
  • JME (Juvenile Myoclonic Epilepsy)
  • JMEs (Juvenile Myoclonic Epilepsy)
  • Myoclonic Epilepsy, Adolescent
  • Epilepsy, Adolescent Myoclonic
  • Petit Mal, Impulsive, Janz
  • Myoclonic Epilepsy, Juvenile, 1
  • Petit Mal, Impulsive
  • Epilepsy, Myoclonic Juvenile
  • Juvenile Epilepsy, Myoclonic
  • Myoclonic Juvenile Epilepsy
  • Adolescent Myoclonic Epilepsy
  • Epilepsy, Myoclonic, Juvenile
早前的内容:
  • Epilepsies, Myoclonic (1977-1999)
  • Epilepsy, Absence (1975-1999)
  • Myoclonus (1975-1999)

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