Children’s Craniofacial Association (CCA)
2025 Member
About Children’s Craniofacial Association (CCA)
Children’s Craniofacial Association is a national, 501(c)3 nonprofit organization, headquartered in Dallas, Texas. Nationally and internationally, CCA addresses the medical, financial, psychosocial, emotional, and educational concerns relating to craniofacial conditions. CCA’s services include providing a list of qualified Craniofacial Centers, family networking, an annual family retreat, financial assistance for food travel and lodging for families who must travel for quality care, and we publish a newsletter and syndrome booklets as well as overviews addressing concerns related to having facial differences. CCA’s mission is to empower and give hope to individuals and families affected by facial differences.
Related Rare Diseases:
- Síndrome trico-dento-óseo
- Síndrome de Treacher Collins
- Síndrome de megalocórnea-discapacidad intelectual
- Síndrome de Binder
- Síndrome de Primrose
- Pfeiffer Syndrome
- Hallermann-Streiff Syndrome
- Setleis Syndrome
- Costello Syndrome
- Scott Craniodigital Syndrome
- IRF6-Related Disorders
- Craniofrontonasal Dysplasia
- Orocraniodigital Syndrome
- Gorlin-Chaudhry-Moss Syndrome
- Kenny-Caffey Syndrome
- KBG Syndrome
- Pycnodysostosis
- Summitt Syndrome
- Sakati Syndrome
- Goodman Syndrome
- Ring Chromosome 4
- Chromosome 15 Ring
- Chromosome 18q- Syndrome
- Fryns Syndrome
- Chromosome 18 Ring
- Chromosome 9 Ring
- Primary Craniosynostosis
- Chromosome 6 Ring
- Frontofacionasal Dysplasia
- Maxillofacial Dysostosis
- Pallister W Syndrome
- Nager Syndrome
- Miller Syndrome
- Marshall Syndrome
- Otopalatodigital Syndrome Type I and II
- Cardiofaciocutaneous Syndrome
- Hyperostosis Frontalis Interna
- Encephalocele
- Fibrous Dysplasia
- Frontonasal Dysplasia
- Fraser Syndrome
- Robinow Syndrome
- Pierre Robin Sequence
- Cerebro Oculo Facio Skeletal Syndrome
- Larsen Syndrome
- Seckel Syndrome
- Rubinstein-Taybi Syndrome
- Moebius Syndrome
- Leprechaunism
- Oculo-Auriculo-Vertebral Spectrum
- Saethre Chotzen Syndrome
- Antley-Bixler Syndrome
- Three M Syndrome
- Cornelia de Lange Syndrome
- Síndrome de Melnick-Needles
- Displasia cleidocraneal
- Trastorno del espectro ESCO2
- Síndrome de Muenke
- Síndrome de cefalopolisindactilia de Greig
- Síndrome de Shprintzen-Goldberg
- Síndrome de Simpson-Golabi-Behmel
- Síndrome de Opitz G/BBB ligado al cromosoma X
- Síndrome orofaciodigital
- Pentasomía X
- Síndrome de abléfaron-macrostomía
- Síndrome de Aarskog
- Síndrome de Jackson-Weiss
- Síndrome de Hajdu Cheney
- Bent Bone Dysplasia Syndrome