Treacher Collins Syndrome in Children

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Contact the Cleft and Craniofacial Center


Treacher Collins syndrome is a genetic birth disorder characterized by the premature joining of certain bones of the skull during development, which affects the shape of the head and face.

  • Most children with Treacher Collins syndrome are of normal intelligence.
  • Common features of this syndrome include:
    • down-slanting eyes
    • underdevelopment of or absence of cheekbones
    • lower jaw is often small
    • underdeveloped or unusually formed ears
    • possible cleft palate

A team approach to Treacher Collins syndrome

The Cleft and Craniofacial Program at Boston Children's Hospital provides a team approach to the evaluation, diagnosis and treatment of children and adults with congenital or acquired facial deformities. If your child has been diagnosed with Treacher Collins syndrome, our doctors can help.

And if you're pregnant and have a family history of Treacher Collins syndrome, you can talk to one of our genetic counselors for advice.

We are grateful to have been ranked #1 on U.S. News & World Report's list of the best children's hospitals in the nation for the third year in a row, an honor we could not have achieved without the patients and families who inspire us to do our very best for them. Thanks to you, Boston Children's is a place where we can write the greatest children's stories ever told.”
- Sandra L. Fenwick, President and CEO

Boston Children's Hospital
300 Longwood Avenue, Boston, MA 02115
For Patients: 617-355-6000
For Referring Providers: 844-BCH-PEDS | 844-224-7337