Severe myoclonic epilepsy in infants (SME) is one of the epileptic syndrome with onset in the first year of life with a severe outcome characterized by persistence of fits and delay in psychomotor development. We report the clinical and electroencephalografic characteristics of two children affected by SME who presented a complete control of the seizures still present at the moment of last evaluation.
|Translated title of the contribution||Severe myoclonic epilepsy: Benign evolution in two cases|
|Number of pages||4|
|Journal||Bollettino - Lega Italiana contro l'Epilessia|
|Publication status||Published - 1996|
ASJC Scopus subject areas
- Clinical Neurology