Congenital bilateral perisylvian syndrome with hydrocephalus
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Salih Hattapoğlu, Cihad Hamidi 1 * , Cemil Göya, Mehmet Guli Çetinçakmak, Memik Teke
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1 Dicle Üniversitesi Tıp Fakültesi, Radyoloji Anabilim Dalı, Diyarbakır, Turkey* Corresponding Author

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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This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Article Type: Case Report

J Clin Exp Invest, 2012, Volume 3, Issue 4, 552-554

https://doi.org/10.5799/ahinjs.01.2012.04.0222

Publication date: 13 Dec 2012

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Article Downloads: 1128

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