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Myoclonic Epilepsy, Juvenile

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Definition: 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)      Other names Syndrome, Janz; Petit Mals, Impulsive; Myoclonic Epilepsies, Juvenile; Myoclonic Epilepsies, Adolescent; Juvenile Myoclonic Epilepsies; JMEs (Juvenile Myoclonic Epilepsy); Epilepsy, Juvenile Myoclonic; Epilepsy, Adolescent Myoclonic; Epilepsies, Juvenile Myoclonic; Epilepsies, Adolescent Myoclonic; Adolescent Myoclonic Epilepsy; Adolescent Myoclonic Epilepsies; Petit Mal, Impulsive, Janz; Petit Mal, Impulsive; Myoclonic Epilepsy, Juvenile, 1; Myoclonic Epilepsy, Adolescent; Juvenile Myoclonic Epilepsy of Janz; Janz Juvenile Myoclonic Epilepsy; Janz Impulsive Petit Mal; JME (Juvenile Myoclonic Epilepsy)
 
SubstanceCAS Registry & nameCategoriesSource
EFHC1 protein, human  0   *Calcium-Binding Proteins Myoclonic Epilepsy, Juvenile EF Hand Motifs. Nat Genet 2004 Aug;36(8):842-9

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Sources: NLM Medical Subject Headings, NIH UMLS, Drugs@FDA, FDA AERS original data copyright United States Government. No endorsement implied. Last modified 6/6/2012

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