Dental phenotype in an adolescent with osteogenesis imperfecta type XII
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DOI: 10.1136/bcr-2021-246554
Abstract: Mutation in SP7, encoding the osteoblast-specific transcription factor SP7 (also known as osterix), has been described to cause osteogenesis imperfecta (OI) type XII. However, the exact dental phenotype has not been well described. We report… read more here.
Keywords: type xii; xii; imperfecta type; dental phenotype ... See more keywords