
This study aimed to examine the prevalence of WNT10A and RUNX2 mutations and assess their potential impact on the phenotype of non‐syndromic tooth agenesis. The trend of increasing WNT10A mutations and a slight increase in RUNX2 conversions were revealed in tooth agenesis cases compared to unaffected family members in this study. In addition, there was a higher prevalence of hypodontia than oligodontia, increased frequency of females over males with missing teeth, and a wide phenotypic variability was observed in individuals and families analyzed. Thus, these findings highlight the critical role of WNT10A and RUNX2 mutations in the genetic aetiology of non‐syndromic tooth agenesis.
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