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 Facial features include widely spaced eyes, bulging of the eyes, an underdeveloped and ‘sunken-in’ appearance of the mid-face, and/or narrow roof of the mouth. This condition may also involve complex webbing (syndactyly) of the hands and feet.

Causes of Apert Syndrome

Apert Syndrome is a very rare genetic disorder. The incidence of children born with this disease can be 1 in 65,000 to 1 in 160,000. It can be passed on from the child’s parents through autosomal dominant inheritance. This means that only one parent needs to have the abnormal gene for the child to inherit the disease. The majority of cases are not inherited, which means that there was a new mutation in the child’s fibroblast growth factor receptor 2 gene, located on chromosome 10.

Treatment of Apert Syndrome

Apert Syndrome is a complex condition that requires multiple stages of treatment over the course of the patient’s lifetime. Craniosynostosis is treated by performing surgery to the skull. Oftentimes, the upper and middle face will require surgery as well. The first goal is to open the closed sutures to prevent problems with high pressure in the brain and allow the brain to grow normally. The second goal is to obtain a normal shape of the skull and face. 

The timing and type of surgery your child will have depends on your child’s condition and your surgeon. Your surgeon will also discuss the timing of hand and feet syndactyly release. Our comprehensive and specialized team includes a geneticist, craniofacial plastic surgeon, pediatric neurosurgeon, and dental specialists who will care for your child every step of the way. To learn more about Apert syndrome treatment in Richmond, VA, please call to schedule an appointment with one of our craniofacial surgeons.

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