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Progressive myoclonic epilepsy

Orpha number ORPHA98261
Synonym(s) PME
Progressive myoclonus epilepsy
Prevalence -
Inheritance -
Age of onset -
ICD-10 -
OMIM -
UMLS
  • C0751778
MeSH
  • D020191
MedDRA -
SNOMED CT
  • 267581004

Summary

An Orphanet summary for this disease is currently under development. However, other data related to the disease are accessible from the Additional Information menu located on the right side of this page.


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Detailed information

Emergency guidelines
  • FR (2013,pdf)
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