Apert Syndrome
Apert syndrome (Acrocephalosyndactyly) is a rare genetic disorder characterized by the premature fusion of certain skull bones, leading to distinct facial and cranial abnormalities. This condition, also known as acrocephalosyndactyly, impacts skull shape, facial appearance, and can cause webbed fingers and toes (syndactyly). Named after French physician Eugène Apert, who…
