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)
Year introduced: 2000
PubMed search builder options
Subheadings:
Tree Number(s): C10.228.140.490.375.130.670, C10.228.140.490.493.063.670
MeSH Unique ID: D020190
Entry Terms:
- 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
Previous Indexing: