Epilessia notturna del lobo frontale in un caso di aspartilglucosaminuria

Translated title of the contribution: Nocturnal frontal lobe epilepsy in a patient with aspartylglucosaminuria

M. Santucci, V. Gentile

Research output: Contribution to journalArticlepeer-review

Abstract

We described a 26-year-old Italian man with a definite diagnosis of aspartylglucosaminuria, a lysosomal storage disease, frequent in the Finnish population, with a high occurrence of epileptic seizures. At the age of 24 years he began to present, during sleep, events characterized by stereotyped paroxysmal agitated motor behaviour, that recurred many times a night. The video-EEG recording of the episodes supported the diagnosis of nocturnal frontal lobe epilepsy.

Translated title of the contributionNocturnal frontal lobe epilepsy in a patient with aspartylglucosaminuria
Original languageItalian
Pages (from-to)161-163
Number of pages3
JournalBollettino - Lega Italiana contro l'Epilessia
Issue number125-126
Publication statusPublished - Jul 2004

ASJC Scopus subject areas

  • Clinical Neurology

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