Children's hospitals for craniofacial care

Twelve nationally and internationally recognized children’s hospitals known for surgical innovation, multidisciplinary treatment and family-centered support in craniofacial and craniosynostosis care.

These programs lead the field in craniofacial surgery and care. Several of them, including Nicklaus Children’s, Johns Hopkins, CHOP and University of Michigan Health, are also organizations we have funded on behalf of families .

Leading craniofacial and craniosynostosis programs

  • Children's Hospital of Philadelphia

    Craniofacial Program

    One of the largest and most experienced craniofacial programs in the world, known for pioneering surgical techniques and comprehensive diagnostic care.

    www.chop.edu
  • Boston Children's Hospital

    Cleft and Craniofacial Center

    State-of-the-art surgical treatment for craniosynostosis and complex craniofacial anomalies, supported by extensive research and multidisciplinary specialists.

    www.childrenshospital.org
  • St. Louis Children's Hospital

    Cleft Palate and Craniofacial Institute

    Internationally recognized for pioneering minimally invasive endoscopic craniosynostosis repairs with exceptional safety outcomes.

    www.stlouischildrens.org
  • Children's Hospital Los Angeles

    Craniosynostosis Program

    One of the largest craniosynostosis centers on the West Coast, offering high-volume multidisciplinary care including advanced endoscopic procedures for infants.

    www.chla.org
  • UCSF Benioff Children's Hospitals

    Pediatric Craniofacial Center

    Treats a wide range of craniofacial syndromes such as Apert and Crouzon through a highly coordinated multidisciplinary team.

    www.ucsfbenioffchildrens.org
  • Nationwide Children's Hospital (Columbus, OH)

    Center for Complex Craniofacial Disorders

    Personalized, interdisciplinary care for craniosynostosis, plagiocephaly, Pierre Robin sequence and jaw disorders, integrating surgery, ENT, orthodontics and psychology.

    www.nationwidechildrens.org
  • Children's National Hospital (Washington, DC)

    Cleft and Craniofacial Program

    Coordinated craniofacial care through multiple pediatric specialties in a single, streamlined treatment pathway.

    childrensnational.org
  • Cincinnati Children's Hospital Medical Center

    Craniofacial Center

    Ranked among the top U.S. children's hospitals for pediatric neurology and neurosurgery, with expert craniofacial surgery through an elite plastic and neurosurgical team.

    www.cincinnatichildrens.org
  • Seattle Children's Hospital

    Craniofacial Center

    Consistently ranked among the top U.S. children's hospitals, delivering advanced craniofacial and neurosurgical care through interdisciplinary teams.

    www.seattlechildrens.org
  • University of Michigan C.S. Mott Children's Hospital (Ann Arbor, MI)

    Craniofacial Anomalies Program

    Michigan's top-ranked children's hospital, offering exceptional craniofacial surgery within nationally acclaimed neurosurgical programs.

    www.mottchildren.org
  • Children's Hospital of Orange County (CHOC)

    Craniofacial Program

    Comprehensive craniofacial and reconstructive surgery services through an integrated pediatric care network.

    www.choc.org
  • Riley Children's Health (Indianapolis, IN)

    Craniofacial Program

    Advanced craniofacial care supported by top-tier neurosurgical, plastic surgery and genetic expertise.

    www.rileychildrens.org
  • Nicklaus Children's Hospital (Miami, FL)

    Pediatric Craniofacial Center and Clinic

    Florida's only full-service craniofacial center, delivering multidisciplinary care including cranial remodeling, cleft repair, ear reconstruction and orthognathic surgery. Alex Schon had several of his surgeries here.

    www.nicklauschildrens.org

The Alexander Foundation has found these sites helpful. We list them as a starting point, not an endorsement, and we encourage every family to decide for themselves what is useful. Nothing here is medical advice.

Two ways to take the next step

For families

You are not alone in this.

If your child has Cloverleaf Syndrome or another craniofacial condition and the bills are piling up, tell us what is happening. We help where we can, and we will point you to people who can help with the rest.

For supporters

Every dollar reaches a family.

Nobody at the foundation is paid. Apart from minimal supplies and tax filing, every gift goes to families, hospitals, schools and books that change how children treat each other.