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


Figure 1 from Myoclonic status epilepticus in hypoxic ischemic

Figure 2 from A patient with early myoclonic encephalopathy (EME) with

Early Myoclonic Encephalopathy disease Malacards Research Articles

A Case of Myoclonic Epilepsy Presenting with Status Epilepticus in an

(PDF) EarlyOnset Epileptic Encephalopathies Ohtahara Syndrome and