Apert Syndrome – 1 in 65,000 Births

What is Apert Syndrome?: Apert Syndrome, or acrocephalosyndactyly type 1, is a rare congenital disorder characterized by premature fusion of skull sutures, causing distinctive facial and head malformations, as well as fused or webbed fingers and toes. Often featuring a pointed head, sunken midface, connected fingers, and intellectual disability, this condition typically results from random… Read.