AmeriFace
About AmeriFace
The AmeriFace provides information and emotional support to individuals with facial differences. Families are also included as part of its support network. AmeriFace works to increase public understanding through awareness programs and education on behalf of those it serves. AmeriFace welcomes individuals whose facial differences are present at birth, such as cleft lip and palate, Apert, Crouzon, Treacher Collin, microtia, hemangiomas, and Moebius syndrome, as well as other conditions. Others served are those who have differences as a result of illness, disease or trauma, stroke, cancer, accident and fire.
Related Rare Diseases:
- Adams-Oliver Syndrome
- Trismus-Pseudocamptodactyly Syndrome
- Branchio Oculo Facial Syndrome
- Shprintzen Goldberg Syndrome
- Miller Syndrome
- Nager Syndrome
- IRF6-Related Disorders
- Trisomy 9p (Multiple Variants)
- Craniofrontonasal Dysplasia
- Orocraniodigital Syndrome
- Mosaic Trisomy 9
- Pycnodysostosis
- Summitt Syndrome
- Sakati Syndrome
- Goodman Syndrome
- Ring Chromosome 4
- Chromosome 15 Ring
- Chromosome 18q- Syndrome
- Fryns Syndrome
- Chromosome 18 Ring
- Chromosome 9 Ring
- Binder Type Nasomaxillary Dysplasia
- Jackson-Weiss Syndrome
- Primary Craniosynostosis
- Chromosome 6 Ring
- Frontofacionasal Dysplasia
- Baller-Gerold Syndrome
- Maxillofacial Dysostosis
- Pallister W Syndrome
- Encephalocele
- Frontonasal Dysplasia
- Penta X Syndrome
- Fraser Syndrome
- Craniometaphyseal Dysplasia
- Greig Cephalopolysyndactyly Syndrome
- ESCO2 Spectrum Disorder
- Treacher Collins Syndrome
- Carpenter Syndrome
- X-linked Opitz G/BBB Syndrome
- Oral-Facial-Digital Syndrome
- Cerebro Oculo Facio Skeletal Syndrome
- Seckel Syndrome
- Diastrophic Dysplasia
- Moebius Syndrome
- Freeman-Sheldon Syndrome
- Crouzon Syndrome
- Tricho Dento Osseous Syndrome
- Saethre Chotzen Syndrome
- Apert Syndrome
- Trisomía 9 en mosaico
- Síndrome de Crouzon
- Trastorno del espectro ESCO2
- Síndrome de cefalopolisindactilia de Greig
- Síndrome de Shprintzen-Goldberg
- Síndrome de Opitz G/BBB ligado al cromosoma X
- Síndrome orofaciodigital
- Pentasomía X
- Síndrome de Jackson-Weiss
- Síndrome de Apert
