bilateral parasagittal parieto-occipital polymicrogyria

info · Genetic

A polymicrogyria that is characterized by bilateral malformation of cortical development, centered around the parasagittal and mesial aspects of the parietooccipital cortex and that has_material_basis_in homozygous mutation in the FIG4 gene on chromosome 6q21.

Signs and symptoms

Visual hallucination
Focal impaired awareness seizure
Ventriculomegaly
Bilateral tonic-clonic seizure with focal onset
Polymicrogyria
Aggressive behavior
Status epilepticus
Sudden unexpected death in epilepsy
Delirium

Also known as: bilateral temporooccipital polymicrogyria