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Craniofacial Program

If your child has a complex craniofacial condition, Children's Hospital of Philadelphia (CHOP) provides family-centered care from diagnosis through surgery and long-term care. Ours is one of the largest single centers of its kind, with more than 1,200 admissions for surgical procedures each year. This means that our team is highly experienced in treating every kind of difference of the face and skull, from the common to the rare.

Our world-renowned experts have pioneered surgical techniques and serve as consultants to other teams, both nationally and internationally.

Because it can be challenging for a child to deal with a visible difference, we offer your child the highest level of psychological support. We will be with your family every step of the way.

How we serve you

We will give your child the very best care. To do this, we have specialized programs that help children during different stages of their treatment journey. Our goal is to build strong relationships to support you and your child.

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Why choose the Craniofacial Program

Our extensive program offers some treatments and services that other programs might not have. We treat every type of craniofacial condition in children of all ages, including infants. When a child is prenatally diagnosed, we work together with the experts at CHOP's Richard D. Wood Jr. Center for Fetal Diagnosis and Treatment and the Garbose Family Special Delivery Unit to monitor the pregnancy and help the family plan for the arrival of their baby and postnatal treatment options. Our expertise is known the world over.

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Meet your team

Every person on your child’s team has the same goal: to see your child thrive. We provide medical care, emotional support and much more. Each team member has extensive experience in treating children with visible differences.

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Our locations

Get information about the craniofacial care we provide at our Philadelphia hospital.

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Our research

We are constantly striving to make research discoveries that lead to better outcomes for children with craniofacial conditions.

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Our resources

We have gathered resources to give you information and help you find answers to your questions. We hope this makes your family's life a little easier.

Patient stories

Our Stories
Lilliana was born with only one ear due to hemifacial microsomia, a condition in which the tissues on one side of the face are underdeveloped. Doctors at CHOP gave Lilliana a new ear.
Lilliana smiling while riding a swing

Diagnosis and Treatment of Craniofacial Conditions

Learn about the diagnosis and treatment of craniofacial conditions, including craniosynostosis, hemifacial microsomia, and other syndromes.

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