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Tag Archives: Hemifacial Microsomia/Goldenhar Syndrome
What are Craniofacial Anomalies?
Craniofacial anomalies (CFA) are a “diverse group of deformities in the growth of the head and facial bones.” (Lucile Packard Children’s Hospital Stanford) CFAs are present at birth and there are numerous variations which can range from mild to severe … Continue reading
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Tagged Apert Syndrome, CFA, Cleft lip, Cleft palate, craniofacial anomalies, Crouzon Syndrome, Disabilities, disability, frontonasal dysplasia, Hemifacial Microsomia/Goldenhar Syndrome, minorities, NARIC, National Genome Research Institute, National Institutes of Health, NIDRR, NIDRR research, NIH, people with disabilities, Pierre Robin Syndrome, research, Treacher Collins Syndrome
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