Congenital deformity characterized by structural abnormalities of the head and face.
Note: Autosomal dominant mutations have been identified in several genes involved in early development of bone and the tissues of the face, the most frequently implicated being TCOF1.
See also: craniofacial
Source:
PAC, 2016, 88, 713. 'Glossary of terms used in developmental and reproductive toxicology (IUPAC Recommendations 2016)' on page 814 (https://doi.org/10.1515/pac-2015-1202)