{Reference Type}: Case Reports
{Title}: A novel GLI3 frameshift mutation in a Chinese pedigree with polydactyly: A case report.
{Author}: Zhao C;Gao C;Zhu Y;Zhang Q;Lin P;
{Journal}: Heliyon
{Volume}: 10
{Issue}: 7
{Year}: 2024 Apr 15
{Factor}: 3.776
{DOI}: 10.1016/j.heliyon.2024.e28638
{Abstract}: <B>UNASSIGNED: </B>GLI3 gene mutations can result in various forms of polysyndactyly, such as Greig cephalopolysyndactyly syndrome (GCPS, MIM: #175700), Pallister-Hall syndrome (PHS, MIM: #146510), and isolated polydactyly (IPD, MIM: #174200, #174700). Reports on IPD-associated GLI3 mutations are rare. In this study, a novel GLI3 mutation was identified in a Chinese family with IPD.<BR><B>UNASSIGNED: </B>We report a family with six members affected by IPD. The family members demonstrated several special phenotypes, including sex differences, abnormal finger joint development, and different polydactyly types. We identified a novel frameshift variant in the GLI3 gene (NM_000168.6: c.1820_1821del, NP_000159.3: p.Tyr607Cysfs*9) by whole-exome sequencing. Further analysis suggested that this mutation was the cause of polydactyly in this family.<BR><B>UNASSIGNED: </B>The discovery of this novel frameshift variant in our study further solidifies the relationship between IPD and GLI3 and expands the previously established spectrum of GLI3 mutations and associated phenotypes.