Dental and Craniofacial Anomalies Associated with Axenfeld-Rieger Syndrome with PITX2 Mutation

<table>OTP (11 years 3 months) showing agenesis of the upper lateral incisors, taurodontism of the molars, and microdontia with crown hypoplasia of the upper central incisors and congenital missing 18 and 28 in patient 2.</table>

Case Reports in Medicine

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Figure 3: Dental and Craniofacial Anomalies Associated with Axenfeld-Rieger Syndrome with PITX2 Mutation 