Diseases

Juvenile Myoclonic Epilepsy

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)

National Library of MedicineMedical Subject Headings2026

Structured Summary

Abstract

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)

MeSH Record

Classification

Broader headings

Related Concepts

Knowledge Graph

Loading graph…

Drag nodes to rearrange; hover to trace links; click a node to open its page.

MeSH Record

Synonyms

20 entry terms
  • Adolescent Myoclonic Epilepsy
  • Epilepsy, Myoclonic Juvenile
  • Epilepsy, Myoclonic, Juvenile
  • Impulsive Petit Mal Epilepsy
  • Impulsive Petit Mal, Janz
  • JME (Juvenile Myoclonic Epilepsy)
  • Janz Impulsive Petit Mal
  • Janz Juvenile Myoclonic Epilepsy
  • Janz Syndrome
  • Juvenile Myoclonic Epilepsy of Janz
  • Myoclonic Epilepsy, Adolescent
  • Myoclonic Epilepsy, Juvenile
  • Myoclonic Epilepsy, Juvenile, 1
  • Petit Mal, Impulsive
  • Petit Mal, Impulsive, Janz
  • Epilepsy, Adolescent Myoclonic
  • Epilepsy, Juvenile Myoclonic
  • JMEs (Juvenile Myoclonic Epilepsy)
  • Juvenile Epilepsy, Myoclonic
  • Myoclonic Juvenile Epilepsy

MeSH Record

Aspects Covered

35 allowable subheadings

Indexed with the subheadings blood, cerebrospinal fluid, chemically induced, classification, complications, congenital, diagnosis, diagnostic imaging, diet therapy, drug therapy, economics, embryology, enzymology, epidemiology, ethnology, etiology, genetics, history, immunology, metabolism, microbiology, mortality, nursing, parasitology, pathology, physiopathology, prevention & control, psychology, radiotherapy, rehabilitation, surgery, therapy, urine, veterinary, virology.

MeSH Record

History Note

2000

MeSH Record

Previous Indexing

  • Epilepsies, Myoclonic (1977-1999)
  • Epilepsy, Absence (1975-1999)
  • Myoclonus (1975-1999)

MeSH Hierarchy

Tree Numbers

AMA Style

References

  1. National Library of Medicine. Juvenile Myoclonic Epilepsy. Medical Subject Headings (MeSH). 2026. Unique ID D020190. http://id.nlm.nih.gov/mesh/2026/D020190
  2. Juvenile Myoclonic Epilepsy. In: Wikipedia. https://en.wikipedia.org/wiki/Juvenile_myoclonic_epilepsy
  3. Juvenile Myoclonic Epilepsy. In: Wikidata. https://www.wikidata.org/wiki/Q543517