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Our Craniofacial team is one of the largest in the nation — and one of the most respected. That’s because our craniofacial specialists tailor a unique plan of care for every child we see, with an emphasis on providing all aspects of care to treat the whole child.
Our Craniofacial team are experts in diagnosing and treating craniosynostosis. Watch our video series to learn more about craniosynostosis at Seattle Children’s.
No parent wants to go to the world’s second-best craniofacial team.
Kids with facial paralysis may be unable to smile, frown or close their eyes. Our experts can help restore facial movements.
On staff since June 1991
Meet the Craniofacial team.
On staff since September 2001
We have the specialized training to use nasoalveolar molding before cleft lip and palate surgery – a technique that may mean fewer surgeries.
Learn more about clinical advances
We have a great deal of experience caring for children with craniosynostosis. Each year we evaluate about 80 new children with craniosynostosis and perform about 90 surgeries to correct this condition.
Learn more about craniosynostosis
The collaboration between our research and clinical teams is bringing knowledge from the laboratory to the bedside in the form of improved procedures and better devices.
Learn more about the Center for Craniofacial Research
We’re dedicated to the care of children with craniofacial conditions. Our team of 48 providers from 19 specialties provides diagnosis and long-term management for children of all ages and developmental stages.
Learn more about us
Research teams with the Craniofacial Center work to find the causes of craniofacial conditions and develop new methods to prevent, diagnose and treat them.
Clinical and translational research takes discoveries made in the laboratory and translates them into therapies that people can actually use in daily life.
Our mission is to restore children's health after injury through repair, regeneration or replacement of tissues, cells and organs.
Our researchers are creating a future where doctors can use genetic information to identify, plan for and maybe even correct genetic defects while a child is still in utero.
We’re laying the foundation for innovative therapies that may prevent or cure neurological, neurodevelopmental and neuropsychiatric disorders.
We are a national leader in treating all craniofacial conditions – from the simplest to the most complex.
We're on a quest to help families by identifying treatments for craniofacial microsomiat that work best.
A revolutionary procedure developed by our surgical team normalizes the facial proportions of children with Apert syndrome.
Grayson was born with metopic craniosynostosis, which is a relatively rare condition where the front of his skull was fused ... cont.
Thenumber three rating goes to Seattle Children’s. Prioritizing specialty care and patient safety make Seattle Children’s a ... cont.
International team finds genes associated with condition that causes premature skull fusion
Two Distinct Mutations Cause “Question Mark Ears Syndrome,” Study Finds
Seattle, Longview and Tri-Cities206-987-2208
Learn more about visiting the Craniofacial Center
Seattle Children’s bills a facility charge (PDF) for hospital-based clinic visits.
Each year, hundreds of kids like Abigael receive the region’s most advanced pediatric care for head and face abnormalities from Children’s Craniofacial team. Your support makes it possible.
Seattle Children’s provides healthcare without regard to race, color, religion (creed), sex, gender identity or expression, sexual orientation, national origin (ancestry) or disability. Financial assistance for medically necessary services is based on family income and hospital resources and is provided to children under age 21 whose primary residence is in Washington, Alaska, Montana or Idaho.
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