Kristofer Andersson
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Dentinogenesis imperfecta type II in Swedish children and adolescents Open
These results show a significantly lower prevalence of DGI type II than previously reported and point to the importance of excluding OI in children with DGI.
Prevalence of dentinogenesis imperfecta and dental aberrations related to genetic findings in osteogenesis imperfecta Open
Osteogenesis imperfecta (OI) is a clinically and genetically heterogeneous connective tissue disorder, mainly caused by mutations in COL1A1 and COL1A2, the genes encoding collagen type I. The cardinal symptoms include bone fragility and va…
View article: Mutations in COL1A1 and COL1A2 and dental aberrations in children and adolescents with osteogenesis imperfecta – A retrospective cohort study
Mutations in COL1A1 and COL1A2 and dental aberrations in children and adolescents with osteogenesis imperfecta – A retrospective cohort study Open
Osteogenesis imperfecta (OI) is a heterogeneous group of disorders of connective tissue, caused mainly by mutations in the collagen I genes (COL1A1 and COL1A2). Dentinogenesis imperfecta (DGI) and other dental aberrations are common featur…