How to choose a plastic and reconstructive surgery program for craniofacial conditions: A guide for parents
Important questions to ask potential providers when looking for a program to treat your child’s craniofacial difference.
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Important questions to ask potential providers when looking for a program to treat your child’s craniofacial difference.
The Face to Face Portrait Project creates portraits of children and adolescents with craniofacial conditions to help them see themselves in a different light.
Philly Phaces provides peer support, advocacy, and resources to help Philadelphia-area children facing appearance differences from craniofacial abnormalities and cleft lip and palate.
March of Dimes is an international organization that works to prevent birth defects, premature birth, and infant mortality and to support expectant and new parents.
Learn more about craniosynostosis and surgical treatment for the condition.
Learn more about jaw surgery and how it's managed at CHOP.
The American College of Allergy, Asthma & Immunology provides information and resources about allergies and asthma for patients and families.
The A-T Children’s Project is a 501c3 nonprofit organization that raises funds to support and coordinate biomedical research projects, scientific conferences and a clinical center aimed at finding life-improving therapies and a cure for ataxia-telangiectasia (A-T).
The American Society of Plastic Surgeons (ASPS) offers information about cleft lip and cleft palate repairs.
The Children's Craniofacial Association empowers and gives hope to individuals and families affected by facial differences.