Early myoclonic encephalopathy [1] | |
---|---|
Specialty | Neurology |
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]
The prevalence estimates among EME are of <1 / 1 000 000. [5]
{{
cite web}}
: CS1 maint: numeric names: authors list (
link)
Early myoclonic encephalopathy [1] | |
---|---|
Specialty | Neurology |
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]
The prevalence estimates among EME are of <1 / 1 000 000. [5]
{{
cite web}}
: CS1 maint: numeric names: authors list (
link)