Early myoclonic encephalopathy

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. 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.

Epidemiology

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

References

External links

1. Encephalopathy
2. Ohtahara syndrome
3. Opsoclonus myoclonus syndrome
4. Myoclonus
5. Glycine encephalopathy
6. Spike-and-wave
7. Dravet syndrome
8. Progressive myoclonus epilepsy
9. EME
10. Creutzfeldt–Jakob disease
11. MELAS syndrome
12. Myoclonic astatic epilepsy
13. Epilepsy and employment
14. Epilepsy syndromes
15. Malignant migrating partial seizures in infancy
16. SLC6A1 epileptic encephalopathy
17. Epilepsy
18. SYNGAP1-related intellectual disability
19. SLC25A22
20. GABRB2