What does Apert syndrome look like?

The abnormal skull and facial growth in Apert syndrome produce its main signs and symptoms: A head that is long, with a high forehead. Wide-set, bulging eyes, often with poorly-closing eyelids. A sunken middle face.

What are symptoms of Apert syndrome?

What does Apert syndrome do to you?

Apert syndrome is characterized by craniosynostosis, a condition in which the fibrous joints (sutures) between bones of the skull close prematurely. This can cause the top of the head to appear pointed and can affect facial bones. Certain fingers or toes may be fused or webbed.

Is Apert fatal?

Life expectancy for an individual with Apert syndrome is normal; however, some of the health problems associated with the syndrome can lead to complicated disease and a premature death.

How long do kids with Apert syndrome live?

Life expectancy also varies between children with Apert syndrome. Those with Apert syndrome who survive past childhood and don't have heart problems likely have a normal or near-normal life expectancy. Life expectancy is likely improving because of advances in surgical techniques and follow-up care.

Michael's Apert Syndrome Journey at Gillette Children's

Who is most likely to get Apert?

Apert syndrome affects an estimated 1 in 65,000 to 88,000 newborns. Although parents of all ages can have a child with Apert syndrome, the risk is increased in older fathers.

Can people with Apert syndrome talk?

Conclusion: Children with Apert syndrome are at a higher risk of speech and language difficulties than the typical population. Speech and Language Therapists play an integral role in the management of school aged children with Apert Syndrome.

Is Apert syndrome a disability?

There is no disability listing for Apert syndrome among the Social Security Administration's (SSA's) impairment list. This does not however mean that the condition cannot medically qualify a child to receive benefits.

Does Apert syndrome cause mental retardation?

Abstract. Apert syndrome is characterized by craniosynostosis, symmetric syndactyly and other systemic malformations, with mental retardation usually present.

What does Apert mean?

Definition of apert

1 archaic : open, manifest, evident. 2 obsolete : bold, straightforward, outspoken.

What are other names for Apert syndrome?

Apert syndrome, also called acrocephalosyndactyly, is a genetic syndrome characterized by anomalies of the skull, face and limbs.

Can you cure Apert syndrome?

Apert syndrome is a lifelong condition with no cure. Surgery to release pressure to the brain, along with reconstructive surgery, will occur soon after your baby is born.

Is Apert syndrome hereditary?

Disease at a Glance

Apert syndrome is caused by a change in the FGFR2 gene. It is inherited in an autosomal dominant manner, but many cases result from a new genetic change in a person with no family history of the disorder (a de novo genetic change).