Early myoclonic encephalopathy (EME) is a rare neonatal-onsetepilepsy 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]
^Berg, AT; Berkovic, SF; Brodie, MJ; Buchhalter, J; Cross, JH; et al. (Apr 2010). "Revised terminology and concepts for organization of seizures and epilepsies: report of the ILAE Commission on Classification and Terminology, 2005-2009".Epilepsia.51 (4):676–85.doi:10.1111/j.1528-1167.2010.02522.x.PMID20196795.
^Guerrini, R; Aicardi, J (November 2003). "Epileptic encephalopathies with myoclonic seizures in infants and children (severe myoclonic epilepsy and myoclonic-astatic epilepsy)".Journal of Clinical Neurophysiology.20 (6):449–61.doi:10.1097/00004691-200311000-00007.PMID14734934.S2CID20217683.
