Whole exome sequencing identified a novel frameshift variant in the BHLHA9 in an Iranian family with mesoaxial synostotic syndactyly

Abstract

Mesoaxial synostotic syndactyly with phalangeal reduction (MSSD) represents a rare non-syndromic defect with an autosomal recessive pattern of inheritance. Sequence variants in the BHLHA9 gene cause MSSD and to date only a few mutations in this gene have been reported. In the present report, we have described a consanguineous Iranian family segregating MSSD in an autosomal recessive manner. The family had two affected siblings showing evidence of camptodactyly in some fingers, complete syndactyly of the 3rd and 4th fingers with synostoses of the corresponding metacarpals, and associated single phalanx in both right and left hand. Whole exome sequencing (WES) followed by segregation analysis using Sanger sequencing identified a novel homozygous frameshift variation [c.74_74delG p.(G25Afs*55)] in the BHLHA9 gene. This has expanded the spectrum of mutations in the BHLHA9 and will facilitate genetic counseling in Iranian families segregating MSSD-related phenotypes.

Recent Advances in Syndactyly: Basis, Current Status and Future Perspectives

“…Likewise, a mutation in BHLHA9 present on chromosome 17q13.3 has been linked with the SD9 [32]. Several other studies have reported missense (c.311T>C;p.I104T), frameshift (c.74delG;p.G25Afs*55), and deletion (c.252_270delinsGCA;p.F85Qfs*108) variants in the BHLHA9 (Reference sequence: NM_001164405.2) in families affected with SD9 [33,57,58].…”