Congenital bilateral perisylvian syndrome with hydrocephalus

Year 2012, , 552 - 554, 01.12.2012

Salih Hattapoğlu Cihad Hamidi Cemil Göya Mehmet Guli Çetinçakmak Memik Teke

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

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.

Keywords

Epilepsy, congenital bilateral perisylvian syndrome, polymicrogyria, hydrocephalus, pseudobulbar palsy

Hidrosefali ile birlikte seyreden bilateral konjenital perisilviyan sendrom

Abstract

Konjenital bilateral slyvian sendrom (KBPS) mental retardasyon, epilepsi, konuşma bozukluğu, psödobulbar palsi gibi bulgularla kendini gösteren, genetik ve genetik dışı nedenlerle ortaya çıkan konjenital bir hastalıktır. Klinik bulgularla birlikte, MR görüntüleme ile karakteristik bulguların (polimikrogiri gibi) ortaya konması, tanı konulmasında katkı sağlamaktadır. Yazımızda hidrosefali bulgusu bulunan KBPS tanısı konulan 18 aylık kız çocuğu olgusunu sunmayı amaçladık.

Keywords

Epilepsi, konjenital perisilvian sendrom, polimikrogri, hidrosefali, psödobulbar palsi

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