FACES: The National Craniofacial Association

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:

• Melnick Needles Syndrome
• Adams-Oliver Syndrome
• Trismus-Pseudocamptodactyly Syndrome
• Shprintzen Goldberg Syndrome
• Hajdu Cheney Syndrome
• Hallermann-Streiff Syndrome
• Ablepharon-Macrostomia 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
• Simpson-Golabi-Behmel Syndrome
• Cleidocranial Dysplasia
• Fryns Syndrome
• Binder Type Nasomaxillary Dysplasia
• Jackson-Weiss Syndrome
• Primary Craniosynostosis
• Frontofacionasal Dysplasia
• C Syndrome
• Baller-Gerold Syndrome
• Maxillofacial Dysostosis
• Pallister W Syndrome
• Nager Syndrome
• Miller Syndrome
• Otopalatodigital Syndrome Type I and II
• Hyperostosis Frontalis Interna
• Encephalocele
• Chromosome 22q11.2 Deletion Syndrome
• Frontonasal Dysplasia
• Fraser Syndrome
• Craniometaphyseal Dysplasia
• Branchio Oculo Facial Syndrome
• Greig Cephalopolysyndactyly Syndrome
• ESCO2 Spectrum Disorder
• Pierre Robin Sequence
• Treacher Collins Syndrome
• Carpenter Syndrome
• X-linked Opitz G/BBB Syndrome
• Oral-Facial-Digital Syndrome
• Cerebro Oculo Facio Skeletal Syndrome
• Pfeiffer Syndrome
• Larsen Syndrome
• Rubinstein-Taybi Syndrome
• Moebius Syndrome
• Freeman-Sheldon Syndrome
• Waardenburg Syndrome
• Crouzon Syndrome
• Tricho Dento Osseous Syndrome
• Oculo-Auriculo-Vertebral Spectrum
• Saethre Chotzen Syndrome
• Apert 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
• Muenke Syndrome
• 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
• Primrose Syndrome