The publisher regrets that the author names were printed incorrectly. They are now shown correctly above.
Accepted: February 26, 2004
Received in revised form: February 25, 2004
Received: January 29, 2004
© 2005 Elsevier B.V. Published by Elsevier Inc. All rights reserved.
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- Congenital bilateral perisylvian syndrome with partial epilepsy. Case report with long-term follow-upBrain and DevelopmentVol. 27Issue 1
- PreviewCongenital bilateral perisylvian syndrome (CBPS) is a rare neurological disorder characterised by pseudobulbar palsy, cognitive deficits and epilepsy associated with bilateral perisylvian cortical dysplasia on neuroimaging studies. We report a long-term follow-up of a 18-years girl diagnosed with CBPS according to the typical clinical and magnetic resonance imaging (MRI) features. The patient showed faciopharyngoglossomasticatory diplegia, severe dysarthria, ataxia, spastic quadriparesis and severe mental retardation.