Epilessia mioclonica severa: Evoluzione relativamente benigna in due casi

Translated title of the contribution: Severe myoclonic epilepsy: Benign evolution in two cases

F. Beccaria, P. Veggiotti, L. Farinotti, A. Gatti, G. Papali, G. Lanzi

Research output: Contribution to journalArticle

Abstract

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 contributionSevere myoclonic epilepsy: Benign evolution in two cases
Original languageItalian
Pages (from-to)503-506
Number of pages4
JournalBollettino - Lega Italiana contro l'Epilessia
Issue number95-96
Publication statusPublished - 1996

ASJC Scopus subject areas

  • Clinical Neurology

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  • Cite this

    Beccaria, F., Veggiotti, P., Farinotti, L., Gatti, A., Papali, G., & Lanzi, G. (1996). Epilessia mioclonica severa: Evoluzione relativamente benigna in due casi. Bollettino - Lega Italiana contro l'Epilessia, (95-96), 503-506.