Nocturnal frontal lobe epilepsy in mucopolysaccharidosis

被引:10
作者
Bonanni, Paolo [1 ]
Volzone, Anna [1 ]
Randazzo, Giovanna [1 ]
Antoniazzi, Lisa [1 ]
Rampazzo, Angelica [2 ]
Scarpa, Maurizio [2 ]
Nobili, Lino [3 ]
机构
[1] IRCCS E Medea, Epilepsy & Clin Neurophysiol Unit, I-31015 Conegliano, TV, Italy
[2] Univ Padua, Dept Paediat, I-35100 Padua, Italy
[3] Osped Niguarda Ca Granda, Claudio Munari Epilepsy Surg Ctr, Milan, Italy
关键词
Sleep disturbances; Epilepsy; Mucopolysaccharidosis; SLEEP; PARASOMNIAS; DISORDERS;
D O I
10.1016/j.braindev.2013.12.002
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
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. (C) 2014 The Japanese Society of Child Neurology. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:826 / 829
页数:4
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