| Literature DB >> 24447995 |
Paolo Bonanni1, Anna Volzone2, Giovanna Randazzo2, Lisa Antoniazzi2, Angelica Rampazzo3, Maurizio Scarpa3, Lino Nobili4.
Abstract
Nocturnal frontal lobe epilepsy (NFLE) is an epileptic syndrome that is primarily characterized by seizures with motor signs occurring almost exclusively during sleep. We describe 2 children with mucopolysaccharidosis (MPS) who were referred for significant sleep disturbance. Long term video-EEG monitoring (LT-VEEGM) demonstrated sleep-related hypermotor seizures consistent with NFLE. No case of sleep-related hypermotor seizures has ever been reported to date in MPS. However, differential diagnosis with parasomnias has been previously discussed. The high frequency of frontal lobe seizures causes sleep fragmentation, which may result in sleep disturbances observed in at least a small percentage of MPS patients. We suggest monitoring individuals with MPS using periodic LT-VEEGM, particularly when sleep disorder is present. Moreover, our cases confirm that NFLE in lysosomal storage diseases may occur, and this finding extends the etiologic spectrum of NFLE.Entities:
Keywords: Epilepsy; Mucopolysaccharidosis; Sleep disturbances
Mesh:
Year: 2014 PMID: 24447995 DOI: 10.1016/j.braindev.2013.12.002
Source DB: PubMed Journal: Brain Dev ISSN: 0387-7604 Impact factor: 1.961