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Konjenital bilateral perisilviyan sendrom: olgu sunumu

Congenital bilateral perisylvian syndrome: a case repor

Journal Name:

  • Gülhane Tıp Dergisi

Publication Year:

  • 2009

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Keywords (Original Language):

Author Name
Abstract (2. Language): 
Congenital bilateral perisylvian syndrome is a rare syndrome characterized with mental retardation, speech retardation, pseudobulbar palsy, epilepsy and bilateral neuronal migration defects in the perisylvian area on brain magnetic rezonans imaging. It may be due to genetic or non-genetic reasons. We herein report a case presenting with complex partial seizures, speech retardation, bilateral fascial diplegia and polymicrogyria findings on brain magnetic resonance imaging and diagnosed to have congenital bilateral perisylvian syndrome as it is very rare.
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Abstract (Original Language): 
Konjenital bilateral perisilviyan sendrom, mental retardasyon, konuşma geriliği, psödobulbar palsi, epilepsi ve beyin manyetik rezonans görüntülemede perisilviyan bölgede bilateral nöronal migrasyon bozukluğu ile karakterize, nadir görülen bir sendromdur. Genetik veya genetik olmayan nedenler sonucunda ortaya çıkabileceği bildirilmektedir. Burada kompleks parsiyel nöbetlerle başvurup, konuşma geriliği, bilateral fasiyal dipleji ve beyin manyetik rezonans görüntülemesinde polimikrogri bulguları ile konjenital bilateral perisilviyan sendrom tanısı konulmuş bir olgu çok nadir görülmesi nedeniyle sunulmuştur.
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  • 1
64-66
  • Turkish

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