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Pediatric Cleft and Craniofacial Center
What is Apert Syndrome?
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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 together too early in the life of the baby. Patients with Apert syndrome typically have premature fusion of multiple cranial sutures.
Physical characteristics include:







Besides the physical characteristics, other health risks are
also associated with Apert Syndrome. These conditions and their
severity vary from patient to patient. These conditions can include: