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FACES is the heart and the hub of the

craniofacial community, supporting people with

medical travel, education, and connection.

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CRANIOFACIAL ANOMALIES

Bell's Palsy

Carpenter Syndrome

Cleft Lip and Palate

Cleidocranial Dysplasia

Craniofacial Fibrous Dysplasia

Craniosynostosis

Crouzon Syndrome

Facial Palsy

Freeman Sheldon Syndrome

Goldenhar Syndrome

Gorlin Syndrome

& Basal Cell Nevus Syndrome

PHACE Syndrome

Pierre Robin Sequence

Ramsay Hunt Syndrome

Saethre-Chotzen Syndrome

Stickler Syndrome

Sturge Weber Syndrome

Treacher Collins Syndrome

Vascular Birthmarks:
Hemangiomas

& Vascular Malformations

Velo-Cardio-Facial

Hallermann-Streiff Syndrome

Hemifacial Microsomia

Hydrocephalus

Miller Syndrome

Moebius Syndrome

Nager Syndrome

Nasal Encephaloceles

Neurofibromatosis

Orbital Hypertelorism

Parry-Romberg Syndrome

Pfeiffer Syndrome

FACES: The National Craniofacial Association

PO Box 11082 | Chattanooga, TN 37401 | USA

(800) 332-2373

FACES The National Craniofacial Association is a 501(c)(3) nonprofit organization incorporated under the laws of the State of Tennessee.

Since 1969, FACES: The National Craniofacial Association, has served children and adults throughout the United States with severe craniofacial disorders resulting from birth, injuries, or disease. There is never a charge for any service provided by FACES.
Our program services address three distinct areas:

Client Travel, Public Awareness and Understanding, and Information and Support.

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