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FACES: The National Craniofacial AssociationOrganization URL(s)
faces@faces-cranio.org
Other Contact Information
P.O. Box 11082
800-332-2373 (Voice - Toll-free) DescriptionThe 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. Print ResourcesQuarterly newsletter, available at no charge.
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