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Erratum| Volume 27, ISSUE 4, P318, June 2005

Erratum to “Congenital bilateral perisylvian syndrome with partial epilepsy. Case report with long-term follow-up” [Brain and Development 27(1): 53–57]☆

  • Lucia Margari
    Correspondence
    Corresponding author.
    Affiliations
    Sezione di Neuropsichiatria Infantile, Dipartimento di Scienze Neurologiche e Psichiatriche, Università degli Studi, Azienda Ospedaliera Policlinico, Piazza Giulio Cesare, CP 70124 Bari, Italy
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  • Anna Presicci
    Affiliations
    Sezione di Neuropsichiatria Infantile, Dipartimento di Scienze Neurologiche e Psichiatriche, Università degli Studi, Azienda Ospedaliera Policlinico, Piazza Giulio Cesare, CP 70124 Bari, Italy
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  • Patrizia Ventura
    Affiliations
    Sezione di Neuropsichiatria Infantile, Dipartimento di Scienze Neurologiche e Psichiatriche, Università degli Studi, Azienda Ospedaliera Policlinico, Piazza Giulio Cesare, CP 70124 Bari, Italy
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  • Maura Buttiglione
    Affiliations
    Sezione di Neuropsichiatria Infantile, Dipartimento di Scienze Neurologiche e Psichiatriche, Università degli Studi, Azienda Ospedaliera Policlinico, Piazza Giulio Cesare, CP 70124 Bari, Italy
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  • Cosma Andreula
    Affiliations
    Neuroradiology Service, Department of Neurological and Psychiatric Sciences, University of Bari, Bari, Italy
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  • Tommaso Perniola
    Affiliations
    Sezione di Neuropsichiatria Infantile, Dipartimento di Scienze Neurologiche e Psichiatriche, Università degli Studi, Azienda Ospedaliera Policlinico, Piazza Giulio Cesare, CP 70124 Bari, Italy
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DOI:https://doi.org/10.1016/j.braindev.2005.01.001
Erratum to “Congenital bilateral perisylvian syndrome with partial epilepsy. Case report with long-term follow-up” [Brain and Development 27(1): 53–57]☆
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      Article info

      Publication history

      Accepted: February 26, 2004
      Received in revised form: February 25, 2004
      Received: January 29, 2004

      Identification

      DOI: https://doi.org/10.1016/j.braindev.2005.01.001

      Copyright

      © 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-up
        Brain and DevelopmentVol. 27Issue 1
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          Congenital 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.
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