Dentinogenesis imperfecta type II in Swedish children and adolescents
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DOI: 10.1186/s13023-018-0887-2
Abstract: BackgroundDentinogenesis imperfecta (DGI) is a heritable disorder of dentin. Genetic analyses have found two subgroups in this disorder: DGI type I, a syndromic form associated with osteogenesis imperfecta (OI), and DGI type II, a non-syndromic… read more here.
Keywords: imperfecta; dgi type; children adolescents; type ... See more keywords