FACES THE NATIONAL CRANIOFACIAL ASSOCIATION

FACES furnishes information about craniofacial centers and publishes a brochure which further details the scope of our organization.  FACES provides referrals to other available resources and organizations, maintains up-to-date information on specific diseases or birth defects, and assists in getting families in touch with other families who have a child with the same disorder.  By connecting these families, FACES gives them the means to alleviate the emotional isolation that is often felt by patient and family.  By sharing information and providing support, FACES helps to build a framework in which clients and their families can cope. 
FACES provides information and support networks on each of these anomalies...
 

 

Amniotic Band Syndrome
 

 

Antley Bixler Syndrome
 

 

Apert Syndrome
 

 

Arnold-Chiari Malformation
 

 

Atresia
 

 

Bear-Stevenson Syndrome
 

 

Beckwith-Wiedemann Syndrome
 

 

Binders Syndrome
 

 

Blepharophimosis/ Ptosis Syndrome
 

 

Branchio-Oculo-Facial Syndrome
 

 

Carpenter Syndrome
 

 

Cerebro-Oculo-Facio-Skeletal Syndrome
 

 

Charge Syndrome
 

 

Cleft Lip and Palate
 

 

Cleidocranial Dysostosis
 

 

Craniofrontonasal Dysplasia
 

 

Craniosynostosis
 

 

Craniometaphyseal Dysplasia
 

 

Crouzon Syndrome
 

 

Facial Nerve Palsy
 

 

Facio-Scapulo-Humeral Muscular Dystrophy
 

 

Fraser Syndrome
 

 

Freeman Sheldon Syndrome
 

 

Fronto-Nasal-Dysplasia
 

 

Goldenhar Syndrome or Hemi-facial Microsomia
 

 

Hallermann Streiff Syndrome
 

 

Hemangioma / Port Wine Stain
 

 

Hemihypertrophy
 

 

Hydrocephalus
 

 

Jackson Weiss Syndrome
 

 

Kleeblattschadel
 

 

Microtia
 

 

Moebius
 

 

Muenke Syndrome
 

 

Nager & Miller Syndrome
 

 

Nasal Encephaloceles
 

 

Neurofibromatosis
 

 

Oral-Facial-Digital Syndrome
 

 

Orbital Hypertelorism
 

 

Oto-Palato-Digital Syndrome
 

 

Parry-Romberg Syndrome
 

 

Pfeiffer Syndrome
 

 

Pierre Robin Syndrome
 

 

Roberts Syndrome
 

 

Rubinstein-Taybi Syndrome 
 

 

Saethre-Chotzen Syndrome
 

 

Stickler Syndrome
 

 

Sturge Weber – Hemangioma
 

 

Tesier/Facial Cleft
 

 

Treacher Collins Syndrome
 

 

Velo-Cardio-Facial Syndrome
 

 

Waardenburg Syndrome

FACES Camp is a camp designed for children with any type of craniofacial anomaly such as: Cleft Lip and Palate, Apert Syndrome, Crouzon Syndrome, Pfeiffer Syndrome, Treacher Collins Syndrome, Goldenhar, and many more. The purpose of the camp is to help children with medical needs foster independence by engaging socially with other children experiencing similar medical issues.