Apert syndrome, also called acrocephalosyndactyly, is a genetic syndrome characterized by anomalies of the skull, face and limbs. Gene mutations are responsible for causing the early …

Apert syndrome is a form of acrocephalosyndactyly, a congenital disorder characterized by malformations of the skull, face, hands and feet. It is classified as a branchial arch syndrome, …

Apert syndrome is a complex condition caused by premature fusion, or early closure, of one or more of the sutures (specialized joints between skull bones that expand during normal brain …

At about 6 months, some babies with Apert syndrome need surgery to reshape the skull and give the brain more room. The procedure is called a posterior cranial vault distraction.

Nov 22, 2021 · Apert syndrome is a rare genetic condition that causes a baby's skull, face, feet and hands to form atypically when the skull joints close too soon.

Oct 26, 2023 · Learn about Apert syndrome, a rare genetic disorder that causes abnormal skull development, its symptoms, causes, treatments, and prognosis. Find out how surgery can …

Aug 20, 2025 · Apert syndrome is a rare autosomal dominant disorder characterized by craniosynostosis, craniofacial anomalies, and severe symmetrical syndactyly (cutaneous and …

Apert Syndrome is a genetic disease in which the growth sutures between the skull bones close earlier than normal during prenatal development, affecting the shape of the head and face.

What is Apert syndrome? Apert syndrome, also known as acrocephalosyndactyly, is a genetic disorder that causes fusion of the skull, hands, and feet bones. It is characterized by …

Apert Syndrome, a form of craniosynostosis, is a genetic condition primarily involving distortions of the head and face. Distortions develop when the bone sections of the skull (sutures) fuse …