Also known as: raniosynostosis.
What is non-syndromic craniosynostosis?
When an infant is born, the bones that make up the skull are typically not joined together fully. Craniosynostosis occurs when the skull bones are joined together prematurely. Non-syndromic craniosynostosis means that there is a fusion of skull bones in the head early on that is not associated with a known syndrome.
What causes non-syndromic craniosynostosis?
The cause of non-syndromic craniosynostosis is typically unknown, though genetic factors may play a role.
What are the symptoms of non-syndromic craniosynostosis?
Typically, a slightly unusual appearance of the head or face are the only symptoms of non-syndromic craniosynostosis.
What are non-syndromic craniosynostosis care options?
Many children with non-syndromic craniosynostosis require no treatment. In some cases, surgery is required to treat the complications related to the disease.
Reviewed by: Mislen S Bauer, MD
This page was last updated on: 4/6/2018 8:33:32 AM
From the Newsdesk
Dr. Chad Perlyn and Dr. Mislen Bauer from the Nicklaus Children's Craniofacial Center are committed to helping families and children with apert syndrome. Check out this segment featured on WPLG Local 10.
Families from all around the world traveled to Nicklaus Children’s Hospital in July for an educational conference about Beckwith-Wiedemann Syndrome (BWS), a congenital, genetic condition that can cause premature birth, hypoglycemia, abdominal wall defects, abdominal malignancies and macroglossia (englarged tongue).