Epilepsy and EEG Findings in Males with Fragile X Syndrome
Autor: | Sebastiano A. Musumeci, Raffaele Ferri, G. De Sarro, Maurizio Elia, Randi J Hagerman, Carlo Alberto Tassinari, B. Dalla Bernardina, Paolo Bosco |
---|---|
Rok vydání: | 1999 |
Předmět: |
FMR-1 gene
Adult Male medicine.medical_specialty Pediatrics Adolescent Epilepsy Frontal Lobe Centrotemporal spikes Electroencephalography Diagnosis Differential Central nervous system disease Epilepsy Sex Factors Seizures Fragile X syndrome EEG Genetic model medicine Humans Prospective Studies Age of Onset Child Psychiatry Prospective cohort study Aged Retrospective Studies Intelligence Tests Models Genetic medicine.diagnostic_test Infant Middle Aged medicine.disease Natural history Epilepsy Temporal Lobe Neurology Child Preschool Fragile X Syndrome EEG Findings Neurology (clinical) Psychology Follow-Up Studies |
Zdroj: | Epilepsia. 40:1092-1099 |
ISSN: | 1528-1167 0013-9580 |
Popis: | Summary: Purpose and Methods: One hundred and ninety-two fragile X male patients were investigated for seizures and EEG findings, 168 in a retrospective and 24 in another prospective study, to characterize the natural history of seizures, epilepsy, and EEG abnormalities in males with this syndrome. Results: Seizures were documented in 35 (18.2%) of 192 patients; they never started before the age of 2 years or after the age of 9 years. Seizures were frequently of the complex partial type and less frequently of the partial motor and generalized type. Seizures involving frontal and temporal lobes were commonly seen and were usually well controlled by anticonvulsants. In the majority of young fragile X patients studied, an age-related paroxysmal EEG pattern was found, which showed neurophysiologic characteristics very similar to those of the centrotemporal spikes. Conclusions: These findings confirm that fragile X syndrome can be considered a genetic model of epilepsy. |
Databáze: | OpenAIRE |
Externí odkaz: |