Expanding the Phenotypic Spectrum of Degcags Syndrome: Novel Craniofacial and Oral Findings.

A girl with DEGCAGS syndrome caused by ZNF699 mutations exhibited previously unreported dental and oral features, including talon cusps, taurodontism, hypomineralized primary molars, and signs of bruxism, expanding understanding of this rare genetic disorder's oral presentation.

A plain-English summary of the study's own findings — we don't add our own claims or interpretation. Read the full paper for the complete methods and results, and apply your own clinical judgement.