Craniosynostosis | Children's Health Queensland

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Craniosynostosis happens when one or more of the seams (called sutures) between the bones in a baby's skull close too early.
Your skull is made up of flat, plate-like bones that protect your brain.
In babies, the gaps between each bone are called sutures. There are 4 sutures in a baby's skull.
Usually, these sutures stay open while your baby's brain grows and develops. The sutures eventually fuse together when babies are about 2 years old.
There are 2 types of craniosynostosis:
A single suture craniosynostosis happens in about 1 in every 3000 births.
In children with craniosynostosis, one or more of the sutures (gaps between the bones) close and the bones fuse too early. This causes your baby's head to be out of shape.
Signs that your baby might have craniosynostosis include:
The symptoms of syndromic craniosynostosis may also include:
The cause of craniosynostosis in most babies is not known.
In some cases, it happens because of a genetic syndrome, such as Apert syndrome. But most babies with craniosynostosis do not have a genetic syndrome.
Research into the causes of craniosynostosis that are not related to a genetic syndrome is ongoing.
See your doctor if you have any concerns about the shape or growth of your baby's head.
Craniosynostosis is normally diagnosed in the first few weeks of a baby's life.
If you are concerned about the shape of your baby's head, see your doctor.
Your doctor will ask questions about:
Your doctor will examine your baby's head thoroughly and measure it. They will check for any conditions that could affect your baby's health.
Your baby may have x-rays or CT scans to help confirm the diagnosis. They may have genetic testing using a sample of their blood.
It's best to detect (find) craniosynostosis early so that treatment can start as soon as possible. If your baby has this condition, your doctor will refer them to a specialist paediatric team.
Surgery is the main treatment. The aim is to return the skull to a more typical shape. Surgery also enables your baby's brain to grow and develop normally.
Surgery for craniosynostosis is usually done between the ages of 3 months and 12 months. In rare cases, a child will need further surgery when they're a little older.
Your child will need to see their doctors regularly after surgery, to monitor their head growth and development.
Researchers are currently studying how stem cells might prevent the bones of the skull from fusing too early.
There is no known way of preventing craniosynostosis.
Surgery can help change the shape of the skull and stop craniosynostosis from getting worse as your baby grows.
In some cases of craniosynostosis, there can be problems with:
Support and information are available through Craniofacial Australia.
The Jigsaw Foundation has more information about craniosynostosis.
Genetic Alliance Australia helps families with craniosynostosis connect with each other and provides information about support groups. Call 02 9295 8359 for more information.
You can also call the healthdirect helpline on 1800 022 222 (known as NURSE-ON-CALL in Victoria). A registered nurse is available to speak with you 24 hours a day, 7 days a week.
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Last reviewed: October 2025

