%0 Journal Article
%T Identification of truncated variants in GLI family zinc finger 3 (GLI3) associated with polydactyly.
%A Wang RY
%A Xiong Q
%A Chang SH
%A Jin JY
%A Xiang R
%A Zeng L
%A Yu F
%J J Orthop Surg Res
%V 19
%N 1
%D 2024 Jul 30
%M 39080720
%F 2.677
%R 10.1186/s13018-024-04928-0
%X <B>BACKGROUND: </B>Polydactyly is a prevalent congenital anomaly with an incidence of 2.14 per 1000 live births in China. GLI family zinc finger 3 (GLI3) is a classical causative gene of polydactyly, and serves as a pivotal transcription factor in the hedgehog signaling pathway, regulating the development of the anterior-posterior axis in limbs.<BR><B>METHODS: </B>Three pedigrees of polydactyly patients were enrolled from Hunan Province, China. Pathogenic variants were identified by whole-exome sequencing (WES) and Sanger sequencing.<BR><B>RESULTS: </B>Three variants in GLI3 were identified in three unrelated families, including a novel deletion variant (c.1372del, p.Thr458GlnfsTer44), a novel insertion-deletion (indel) variant (c.1967_1968delinsAA, p.Ser656Ter), and a nonsense variant (c.2374 C > T, p.Arg792Ter). These variants were present exclusively in patients but not in healthy individuals.<BR><B>CONCLUSIONS: </B>We identified three pathogenic GLI3 variants in polydactyly patients, broadening the genetic spectrum of GLI3 and contributing significantly to genetic counseling and diagnosis for polydactyly.