Early myoclonic encephalopathy

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Early myoclonic encephalopathy[1]
SpecialtyNeurology

Early myoclonic encephalopathy (EME) is a rare neonatal-onset epilepsy developmental and epileptic encephalopathy (DEE) with an onset at neonatal period or during the first 3 months of life.[2] This syndrome is now included as part of the Early infantile developmental and epileptic encephalopathy (EIDEE) under the 2022 ILAE (International League Against Epilepsy) syndrome classification.[3][4]

Epidemiology

The prevalence estimates among EME are of <1 / 1 000 000.[5]

References

  1. PMID 20196795
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  2. S2CID 20217683
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  3. ISSN 0013-9580
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  4. S2CID 22914424
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  5. ^ RESERVED, INSERM US14-- ALL RIGHTS. "Orphanet: Early myoclonic encephalopathy". www.orpha.net.{{cite web}}: CS1 maint: numeric names: authors list (link)

External links

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