Callea, MicheleFattori, FabianaYavuz, İzzetBertini, Enrico2024-04-242024-04-242012Callea, M., Fattori, F., Yavuz, İ. ve Bertini, E. (2012). A new phenotypic variant in cleidocranial dysplasia (CCD) associated with mutation c.391C>T of the RUNX2 gene. BMJ Case Reports.1757-790Xhttps://doi.org/10.1136/bcr-12-2011-5422https://hdl.handle.net/11468/23543The RUNX2 gene is a physiological regulatory gene implicated in the development of cleidocranial dysplasia (CCD). A 13-month-old child presented with clinical features of CCD. At the age of 3 years the diagnosis was corroborated by clinical genetic assessment and DNA analysis, revealing a missense mutation p.R131C (c.391C>T) in RUNX2. At the age of 8 years the child was found to have a unique dental phenotype, represented by lack of supernumerary teeth and congenital absence of one tooth. A simple therapeutic approach was adopted, consisting of interceptive orthodontic treatment. The presence of this specific missense mutation in RUNX2, associated with the lack of typical supernumerary teeth may suggest a phenotype-genotype association.eninfo:eu-repo/semantics/openAccessArticle2-s2.0-848721730812322043510.1136/bcr-12-2011-5422Q2