Aicardi Syndrome

Aicardi syndrome is a rare genetic disorder that appears almost always in girls and is characterized by a combination of abnormalities in the brain, the eyes and neurological activity from the first months of life.

Common manifestations: It usually includes early spasms or seizures, partial absence of a structure that connects the two sides of the brain and particularities in the retina.

Common causes: It is related to a genetic alteration linked to the X chromosome that occurs during early development.

Which specialist treats it? The pediatrician detects the first signs and works together with pediatric neurology for comprehensive follow-up. In the presence of seizures or developmental delays in a baby, it is advisable to seek the evaluation of a professional promptly.