Major speech impairment is a cardinal feature of Rett syndrome. Epilepsy, of variable presentation, is also frequently described. We report a girl who presented rapid speech regression while EEG showed continuous spikes and waves during slow sleep. The clinical picture was consistent with Rett syndrome, confirmed by MECP2 mutation R133C. We hypothesized that speech regression was partially related to nocturnal epileptic activity. Several antiepileptic drugs were used unsuccessfully but valproic acid was accompanied by improvement of verbal fluency, social interaction and manual abilities as measured by the Quebec Scale of Adaptive Behaviors and the Rett syndrome adapted Kerr scale. Continuous spikes and waves during slow sleep are unexpecte...
Day time video records of 14 girls with the Rett syndrome (RS) (6-17, mean 7 years) were analysed to...
We have used a novel neurophysiological technique in the NeuroScope system in combination with conve...
Rett syndrome is a rare but severe neurological disorder associated with a mutation in the methyl Cp...
We recorded all-night electroencephalograms (EEGs)/polysomnograms on 2 consecutive nights from 4 chi...
Nine girls with Rett syndrome had 22 electroencephalographic studies performed over 5 years. Ninetee...
Epilepsy often occurs in Rett syndrome and is considered a major problem. The aim of this study was ...
Epilepsy often occurs in Rett syndrome and is considered a major problem. The aim of this study was ...
Continuous spike and wave in slow-wave sleep (CSWS) is an electroencephalographic (EEG) pattern char...
Rett syndrome (RTT), a severe neurodevelopmental disorder caused by MECP2 gene abnormalities, is cha...
Epilepsy is common in Rett syndrome, an X-linked dominant disorder caused by mutations in the MECP2 ...
Background: Rett syndrome is a neurodevelopmental disorder mainly affecting females. It is principal...
Background Rett Syndrome (RS) is a severe neurodevelopmental disorder. Epileptic seizures occur in 8...
Sleep problems are commonly reported in Rett syndrome (RTT); however the electroencephalographic (EE...
Rett syndrome, a neurodegenerative disorder, occurs almost exclusively in female children and has an...
Rett syndrome, a neurodevelopmental disorder affecting mainly females, is caused by a mutation of th...
Day time video records of 14 girls with the Rett syndrome (RS) (6-17, mean 7 years) were analysed to...
We have used a novel neurophysiological technique in the NeuroScope system in combination with conve...
Rett syndrome is a rare but severe neurological disorder associated with a mutation in the methyl Cp...
We recorded all-night electroencephalograms (EEGs)/polysomnograms on 2 consecutive nights from 4 chi...
Nine girls with Rett syndrome had 22 electroencephalographic studies performed over 5 years. Ninetee...
Epilepsy often occurs in Rett syndrome and is considered a major problem. The aim of this study was ...
Epilepsy often occurs in Rett syndrome and is considered a major problem. The aim of this study was ...
Continuous spike and wave in slow-wave sleep (CSWS) is an electroencephalographic (EEG) pattern char...
Rett syndrome (RTT), a severe neurodevelopmental disorder caused by MECP2 gene abnormalities, is cha...
Epilepsy is common in Rett syndrome, an X-linked dominant disorder caused by mutations in the MECP2 ...
Background: Rett syndrome is a neurodevelopmental disorder mainly affecting females. It is principal...
Background Rett Syndrome (RS) is a severe neurodevelopmental disorder. Epileptic seizures occur in 8...
Sleep problems are commonly reported in Rett syndrome (RTT); however the electroencephalographic (EE...
Rett syndrome, a neurodegenerative disorder, occurs almost exclusively in female children and has an...
Rett syndrome, a neurodevelopmental disorder affecting mainly females, is caused by a mutation of th...
Day time video records of 14 girls with the Rett syndrome (RS) (6-17, mean 7 years) were analysed to...
We have used a novel neurophysiological technique in the NeuroScope system in combination with conve...
Rett syndrome is a rare but severe neurological disorder associated with a mutation in the methyl Cp...