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Polymicrogyria, bilateral perisylvian

*Gene map locus Xq27.2-q28
BPP
CBPS
PMGX
Perisylvian syndrome, congenital bilateral
[Clinical features: mental retardation; epilepsy; pseudobulbar palsy; difficulties with expressive speech and feeding]
[Inheritance: most cases are sporadic, X-linked in some patients]

A Locus for Bilateral Perisylvian Polymicrogyria Maps to Xq28
31-year-old man with bilateral posterior sylvian polymicrogyria
7-year-old girl with bilateral perisylvian, lateral parietal, and parieto-occipital polymicrogyria
American Journal of Human Genetics
American Journal of Neuroradiology
American Journal of Neuroradiology

Congenital Perisylvian Syndrome Presenting with Intractable Seizures
Axial (A) and sagittal T1 weighted (B) magnetic resonance images showing bilateral perisylvian polymicrogyria
Electromagnetic function of polymicrogyric cortex in congenital bilateral perisylvian syndrome
Indian Pediatrics
Journal of Medical Genetics
Journal of Neurology, Neurosurgery and Psychiatry

   
Electromagnetic function of polymicrogyric cortex in congenital bilateral perisylvian syndrome
   
Journal of Neurology, Neurosurgery and Psychiatry
   


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Edited by Aldo Campana, July 4, 2014