Bilateral polymicrogyria

An autosomal recessive condition caused by mutation(s) in the ADGRG1 gene, encoding adhesion G-protein coupled receptor G1. It is characterized by motor and cognitive developmental delay, pyramidal signs, and seizures.

Disease Alternative Name

bilateral frontoparietal polymicrogyria
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Dr.B.L.Kapoor Memorial Hospital

Swami Devi Dyal Hospital And Dental College

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