Craniosynostosis is a birth defect that causes the sutures (the soft tissues between the bones of a child’s skull) to fuse too early, causing pressure on the brain. These sutures typically close around two years of age allowing room for the brain to grow before the bones of the skull come together.

This condition causes the baby’s head to have an abnormal shape. If left untreated, other problems can develop due to the lack of space for the growing brain.

The Margaret Hackett Family Program

At UChicago Medicine, our dedicated neurosurgeons are here to help. For more information about craniosynostosis and the resources we have available, please call the Margaret Hackett Family Program (MHFP) at 773-795-0622

Symptoms of Craniosynostosis

The signs of craniosynostosis are usually present at the time of birth. These symptoms include:

  • Abnormal head shape
  • No soft spot on the skull (no fontanelle)
  • Slow growth of head

Causes of Craniosynostosis

The cause of craniosynostosis is unknown. It may be caused by:

  • Abnormal genes passed down from parent to child (inherited)
  • Genetic syndromes or disorders, such as an abnormally small head (microcephaly) or excess cerebrospinal fluid in the brain (hydrocephalus)
  • Metabolic diseases, such as thyroid problem or rickets

If left untreated, the following problems may develop:

  • Blindness
  • Brain damage
  • Delays in learning
  • Developmental delays
  • Feeding problems
  • Hearing loss
  • Increased pressure inside the skull
  • Seizures

Diagnosis and Treatment of Craniosynostosis

Craniosynostosis is diagnosed with a physical exam to feel for hard, bony ridges in your baby’s skull along with several measurements to compare the placement of his or her eyes and ears. Other exams include:

  • X-rays or CT scans
  • Blood work

Treatment for craniosynostosis commonly involves surgery to increase the volume of the skull which reduces pressure on brain and improves the abnormal shape of the head. Surgical intervention during the first year of life ensures that your baby’s brain has room to grow normally.

Plastic and reconstructive surgeon Russell Reid, MD, PhD., with Trish Lawson and her daughter Molly Lawson, 15 months old, at the Duchossois Center for Advanced Medicine (DCAM)

Craniofacial Anomalies Multidisciplinary Program (CAMP)

Our Craniofacial Anomalies Multidisciplinary Program (CAMP), one of the largest in the region, provides a thorough, team-based approach for the evaluation, diagnosis and treatment of children with craniosynostosis.

Learn more about our CAMP program

Request an Appointment

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To speak to someone directly, please call 1-773-702-2123. If you have symptoms of an urgent nature, please call your doctor or go to the emergency room immediately.

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By submitting this form you acknowledge the risk of sending this information by email and agree not to hold the University of Chicago or University of Chicago Medical Center liable for any damages you may incur as a result of the transfer or use of this information. The use or transmittal of this form does not create a physician-contact relationship. More information regarding the confidentiality of this request can be found in our Privacy Policy.