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                  Craniofacial Anomalies

                  Craniofacial Anomalies


                  • Apert Syndrome

                  • Basal Cell Carcinoma Nevoid Syndrome 

                  • (Gorlin Syndrome & Basal Cell Nevus Syndrome)

                  • Carpenter Syndrome

                  • Cleft Lip and Palate

                  • Cleidocranial Dysplasia

                  • Craniofacial Fibrous Dysplasia

                  • Craniosynostosis

                  • Crouzon Syndrome

                  • Facial Palsy

                  • Freeman Sheldon Syndrome

                  • Goldenhar Syndrome

                  • Hallermann-Streiff Syndrome

                  • Hemifacial Microsomia

                  • Hydrocephalus

                  • Microtia

                  • Moebius Syndrome
                  • Nager Syndrome
                  • Miller Syndrome

                  • Nasal Encephaloceles

                  • Neurofibromatosis

                  • Microcephaly

                  • Orbital Hypertelorism

                  • Parry-Romberg Syndrome

                  • Pfeiffer Syndrome

                  • PHACE Syndrome

                  • Pierre Robin Sequence

                  • Saethre-Chotzen Syndrome

                  • Stickler Syndrome

                  • Sturge Weber

                  • Treacher Collins Syndrome

                  • Vascular Birthmarks: Hemangiomas and Vascular Malformations

                  • Velo-Cardio-Facial



                  Office of Rare Diseases - The Genetic and Rare Diseases Information Center
                  rarediseases.info.nih.gov



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                    FACES: The National Craniofacial Association
                    (423) 266-1632 / (800) 332-2373

                    faces@faces-cranio.org
                    P.O. Box 11082, Chattanooga, TN 37401

                    © FACES: The National Craniofacial Association,

                    All rights reserved.


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