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Abstract
Congenital bilateral perisylvian syndrome (CBPS), which is seen by indications of mental retardasyon, epilepsi, speech disorder and pseudobulbar palsy, is a disease which comes up with genetic and non-genetic reasons. Revealing characteristic indications (like polymicrogyria) with MR imaging and clinic indications contributes making diagnosis. In present paper, we aimed to present 18 month girl case report who diagnosed as CBPS with hydrocephali indication.
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