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 contribution | Nocturnal frontal lobe epilepsy in a patient with aspartylglucosaminuria |
|---|---|
| Original language | Italian |
| Pages (from-to) | 161-163 |
| Number of pages | 3 |
| Journal | Bollettino - Lega Italiana contro l'Epilessia |
| Issue number | 125-126 |
| Publication status | Published - Jul 2004 |
ASJC Scopus subject areas
- Clinical Neurology