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Progressive myoclonic epilepsy

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ORPHA:98261

Classification level: Group of disorders

Synonym(s):
  • PME
  • Progressive myoclonus epilepsy

Prevalence: -

Inheritance: -

Age of onset: Adolescent, Childhood, Infancy, Neonatal

ICD-11: 8A61.41

UMLS: C0751778

MeSH: D020191

GARD: 7140

MedDRA: 10089676

Summary

This term does not characterize a disease but a group of diseases. To learn about the diseases included under this term, you can consult the classifications.

Detailed information

Logo ERN: produced/endorsed by ERN(s) Logo FSMR: produced/endorsed by FSMR(s)

General public
Article for general public
Español (2023) - Asociación Nacional de Personas con Epilepsia-ANPE
Guidelines
Emergency guidelines
Français (2013.pdf) - Orphanet Urgences
Additional information

Further information on this disease

Patient-centred resources for this disease

Research activities on this disease

Newborn screening

The documents contained in this website are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.