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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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      Linked Article

      • 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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