Mesial frontal lobe epilepsy: A clinical entity not sufficiently described

Lucia Fusco, Cesare Iani, M. Teresa Faedda, Mario Manfredi, Federico Vigevano, Gianni Ambrosetto, Carlo Ciarmatori, Carlo Alberto Tassinari

Research output: Contribution to journalArticle

Abstract

Mesial frontal lobe epilepsy provokes a complex clinical syndrome characterized by mainly nocturnal occurrence of seizures with stereotyped patterns of repetitive rhythmic movements and diffuse or lateralized postures. Because the EEG is sometimes normal, this syndrome is not always recognized, and these patients risk misdiagnosis and mismanagement. To define guidelines for diagnosis, we describe eight patients with mesial frontal lobe epilepsy and compare them with similar cases reported as mesial frontal lobe epilepsy or given other diagnostic labels, including hysteria and parasomnia.

Original languageEnglish
Pages (from-to)123-135
Number of pages13
JournalJournal of Epilepsy
Volume3
Issue number3
DOIs
Publication statusPublished - 1990

Keywords

  • Epilepsy
  • Hysteria
  • Mesial frontal lobe
  • Parasomnia
  • Seizures

ASJC Scopus subject areas

  • Clinical Neurology
  • Neuroscience(all)

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  • Cite this

    Fusco, L., Iani, C., Faedda, M. T., Manfredi, M., Vigevano, F., Ambrosetto, G., Ciarmatori, C., & Tassinari, C. A. (1990). Mesial frontal lobe epilepsy: A clinical entity not sufficiently described. Journal of Epilepsy, 3(3), 123-135. https://doi.org/10.1016/0896-6974(90)90098-J