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, August 21, 2012