Genetic and environmental factors may lead to abnormal growth of the orofacial skeleton, affecting the overall structure of the face. In this study, we investigated the craniofacial abnormalities in a mouse model for Keutel syndrome, a rare genetic disease caused by loss-of-function mutations in the matrix Gla protein () gene. Keutel syndrome patients show diffuse ectopic calcification of cartilaginous tissues and impaired midface development.
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