Novel DLX3 variant identified in a family with tricho-dento-osseous syndrome

Objectives: To identify DLX3 variants in a Chinese family with typical clinical manifestations of tricho-dentoosseous syndrome (TDO). Design: Sanger sequencing was performed to detect DLX3 variants in the TDO family. Three-dimensional laser scanning microscopy, bioinformatic and conformational analyses were employed to explore the phenotypic characterization and the functional impact. Results: We identified a novel heterozygous variant in the DLX3 gene (c.534G>C; p.Gln178His). Familial co-segregation verified an autosomal dominant inheritance pattern. Bioinformatic prediction demonstrated the deleterious effects of the variant, and DLX3 structure changes suggested the corresponding functional impairments. Conclusions: We identified a variant in the DLX3 gene in an integrated family of Han nationality for the first time. This study expands the variant spectrum of DLX3 and phenotype spectrum of TDO syndrome.

Automated summary

This study identified a DLX3 variant in a Chinese family for the first time and expanded the phenotype spectrum of TDO syndrome.