FACES: The National Craniofacial Association
2024 Member
About FACES: The National Craniofacial Association
The National Craniofacial Association serves children and adults throughout the United States with severe craniofacial differences resulting from birth defects, injuries, or disease through support in client travel, and public awareness and understanding. FACES is dedicated to assisting children & adults who have craniofacial differences resulting from disease, accident, or birth.
Related Rare Diseases:
- Síndrome trico-dento-óseo
- Síndrome de Treacher Collins
- Síndrome de Binder
- Síndrome de Primrose
- Síndrome de Trismo-Pseudocamptodactilia
- Síndrome de Freeman-Sheldon
- Adams-Oliver Syndrome
- Hallermann-Streiff Syndrome
- Johanson-Blizzard Syndrome
- Scott Craniodigital Syndrome
- Craniofrontonasal Dysplasia
- Orocraniodigital Syndrome
- Gorlin-Chaudhry-Moss Syndrome
- Kenny-Caffey Syndrome
- KBG Syndrome
- Hanhart Syndrome
- Summitt Syndrome
- Sakati Syndrome
- Goodman Syndrome
- Bannayan-Riley-Ruvalcaba Syndrome
- Filippi Syndrome
- Fryns Syndrome
- Primary Craniosynostosis
- Frontofacionasal Dysplasia
- Baller-Gerold Syndrome
- Maxillofacial Dysostosis
- Pallister W Syndrome
- Nager Syndrome
- Miller Syndrome
- Otopalatodigital Syndrome Type I and II
- Hyperostosis Frontalis Interna
- Encephalocele
- Frontonasal Dysplasia
- Fraser Syndrome
- Craniometaphyseal Dysplasia
- Branchio Oculo Facial Syndrome
- Pierre Robin Sequence
- Carpenter Syndrome
- Cerebro Oculo Facio Skeletal Syndrome
- Pfeiffer Syndrome
- Larsen Syndrome
- Rubinstein-Taybi Syndrome
- Moebius Syndrome
- Waardenburg Syndrome
- Oculo-Auriculo-Vertebral Spectrum
- Saethre Chotzen Syndrome
- Antley-Bixler Syndrome
- Cornelia de Lange Syndrome
- Síndrome de Melnick-Needles
- Síndrome de deleción del cromosoma 22q11.2
- Displasia cleidocraneal
- Síndrome de Crouzon
- Trastorno del espectro ESCO2
- Síndrome de Muenke
- Síndrome de cefalopolisindactilia de Greig
- Síndrome de Shprintzen-Goldberg
- Síndrome de Simpson-Golabi-Behmel
- Síndrome C
- Síndrome de Opitz G/BBB ligado al cromosoma X
- Síndrome orofaciodigital
- Síndrome de abléfaron-macrostomía
- Síndrome de Jackson-Weiss
- Síndrome de Apert
- Síndrome de Hajdu Cheney