Craniofacial Foundation of America
975 East Third Street
Chattanooga, TN
4237789176
About Craniofacial Foundation of America
The Craniofacial Foundation of America (CFA) is a non-profit organization dedicated to improving the quality of life for individuals and families affected by head and/or facial difference(s) as a result of birth defect, tumor, or trauma-related injury. Established in 1989, the foundation provides financial assistance for food, travel, and lodging expenses to qualified families traveling to the Tennessee Craniofacial Center for evaluation and treatment. The foundation provides support services for both affected individuals and their families including regularly scheduled support group meetings and a parent-to- parent network. CFA also maintains a toll-free hotline and offers educational materials including brochures on “The History of Craniofacial Surgery” and “Post Traumatic Deformities and Facial Reconstruction in Treacher Collins Syndrome.”
Related Rare Diseases:
- Hallermann-Streiff Syndrome
- Miller Syndrome
- Nager Syndrome
- Megalocornea Intellectual Disability Syndrome
- Setleis Syndrome
- Scott Craniodigital Syndrome
- Trisomy 9p (Multiple Variants)
- Mosaic Trisomy 9
- Filippi Syndrome
- Ring Chromosome 4
- Chromosome 15 Ring
- Chromosome 18q- Syndrome
- Fryns Syndrome
- Chromosome 18 Ring
- Chromosome 9 Ring
- Binder Type Nasomaxillary Dysplasia
- Ectrodactyly Ectodermal Dysplasia Cleft Lip/Palate
- Chromosome 6 Ring
- Jansen Type Metaphyseal Chondrodysplasia
- AEC Syndrome
- Penta X Syndrome
- Robinow Syndrome
- Treacher Collins Syndrome
- Seckel Syndrome
- Tricho Dento Osseous Syndrome
- Apert Syndrome
- Three M Syndrome
- Chromosome 11, Partial Monosomy 11q
- Trisomía 9 en mosaico
- Síndrome de Jacobsen (monosomía parcial 11q)
- Pentasomía X
- Síndrome de anquilobléfaron-displasia ectodérmica-fisura labiopalatina
- Síndrome de Apert