FOXG1 Syndrome is a rare neurodevelopmental disorder caused by mutations in the FOXG1 gene, which plays a crucial role in brain development. This syndrome is often considered a congenital variant ...

Patients with FOXG1 syndrome also have an underdeveloped corpus callosum—a thick nerve fiber bundle that connects and transmits information between the right and left sides of the brain, playing a ...

Mutations in this gene can cause FOXG1 syndrome, a rare genetic disorder characterized by structural and functional brain ...