FACES: The National Craniofacial Association
Organization URL(s)
faces@faces-cranio.orgwww.faces-cranio.org
Other Contact Information
P.O. Box 11082
Chattanooga,
TN 37401
800-332-2373 (Voice - Toll-free)
433-266-1632 (Voice)
433-267-3124 (FAX)
Description
The National Craniofacial Association, formerly the Debbie Fox Foundation, was created in 1969 to assist individuals with facial disfigurations and their families. The Association maintains a registry of centers offering corrective surgery for craniofacial deformities. In addition, financial assistance is provided to qualified applicants. A pamphlet describing the Association's services is available. FACES also provides information packets, at no charge, on the following craniofacial disorders: Apert Syndrome; Binders Syndrome; Carpenter Syndrome; C.H.A.R.G.E. Syndrome; Cleft Lip and Palate; Cleidocranial Dysostosis, Craniosynostosis; Craniometaphyseal Dysplasia; Crouzon Syndrome; Freeman Sheldon Syndrome; Frontonasal Dysplasia; Goldenhar Syndrome; Hemifacial Microsomia; Hydrocephalus; Microtia, Moebius Syndrome; Miller Syndrome; Nager Syndrome; Nasal Encephaloceles; Orbital Hypertension; Parry-Romberg Syndrome; Pfeiffer Syndrome; Pierre Robin Sequence; Saethre-Chotzen Syndrome; Stickler Syndrome; Sturge Weber; Treacher Collins Syndrome; Velo-Cardio-Facial Syndrome.
Online Resources
- Apert Syndrome
http://www.faces-cranio.org/Disord/Apert.htm - Cleft Lip and Palate
http://www.faces-cranio.org/Disord/Cleft.htm - Craniofacial Disorders - List of Disorders
http://www.faces-cranio.org/Disord.htm - Craniofacial Medical Centers
http://www.faces-cranio.org/MedCent.htm
Print Resources
Quarterly newsletter, available at no charge.