Epilessia generalizzata idiopatica a tipo assenza con secondaria evoluzione lennox-like: Descrizione di una famiglia

Translated title of the contribution: Absence epilepsy with lennox-like evolution: Report of a family

L. Lapenta, C. Di Bonaventura, J. Fattouch, S. Casciato, M. Fanella, A. Morano, L. Fusco, M. Manfredi, A. Berardelli, A. T. Giallonardo

Research output: Contribution to journalArticle

Abstract

The Idiopathic Generalized Epilepsy (IGE) is a common genetically determined group of syndromes mainly described in children and adolescence with no structural and anatomic cause, usually with an excellent prognosis and good response to therapy. However, IGE may persist in adult life with atypical electro-clinical features (i.e. drug-resistance, GPFA, tonic seizures) or rarely demonstrate a lennox-like evolution with a relative prognosis. We describe a family with four members affected by IGE, in one case with catastrophic evolution.

Original languageItalian
Pages (from-to)132-133
Number of pages2
JournalBollettino - Lega Italiana contro l'Epilessia
Issue number145
Publication statusPublished - Apr 2013

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ASJC Scopus subject areas

  • Clinical Neurology

Cite this

Lapenta, L., Di Bonaventura, C., Fattouch, J., Casciato, S., Fanella, M., Morano, A., Fusco, L., Manfredi, M., Berardelli, A., & Giallonardo, A. T. (2013). Epilessia generalizzata idiopatica a tipo assenza con secondaria evoluzione lennox-like: Descrizione di una famiglia. Bollettino - Lega Italiana contro l'Epilessia, (145), 132-133.