WebMD describes Apert syndrome, a genetic disorder that can cause abnormalities in the formation of the head and other parts of the body.
Apert syndrome is inherited in an autosomal dominant pattern, which means one copy of the altered gene in each cell is sufficient to cause the disorder.
What Is Apert Syndrome? Apert syndrome is a complex condition caused by premature fusion, or early closure, of one or more of the sutures (specialized joints between ...
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 ...
Apert syndrome is named for the French physician who described the syndrome acrocephalosyndactylia in 1906. Apert syndrome is a rare autosomal dominant ...
What is Apert Syndrome? The following was developed from information contained in an article entitled Clinical Assessment and Multispecialty Management of Apert ...
What is Apert Syndrome? Apert Syndrome is a rather rare autosomal dominant disorder described by the French physician named Eugene Apert in 1906.
Apert syndrome is a genetic disease in which the seams between the skull bones close earlier than normal. This affects the shape of the head and face.
Overview. Apert syndrome is a rare genetic condition affecting primarily the skull and facial bones and the limbs. It leads to craniosynostosis, involving the coronal ...
Apert Syndrome. Download PDF information sheet. Back to Craniofacial Anomalies. What is Apert Syndrome? Apert Syndrome is a condition involving distortions of the ...