| Literature DB >> 30945277 |
Muhammad Umair1,2,3, Muhammad Bilal2, Raja H Ali2,4, Bader Alhaddad3, Farooq Ahmad2, Tobias B Haack3, Majid Alfadhel1,5, Muhammad Ansar2, Thomas Meitinger3, Wasim Ahmad2.
Abstract
Pre-axial polydactyly (PPD) is characterized by well-developed non-functional 1st digit (thumb) duplication in hands and/or feet. It is mostly inherited in autosomal dominant manner. In the present study, two families of Pakistani origin, demonstrating unilateral PPD type A, have been characterized at clinical and genetic levels. Whole-exome sequencing (WES) revealed a nonsense mutation (c.84C > A, p.Tyr28*) in the STKLD1, located on chromosome 9q34.2, in affected individuals of both the families. Our findings report the first direct involvement of the STKLD1 in the digit development and highlight the importance of inclusion of this gene for screening individuals presenting non-syndromic recessive PPD.Entities:
Keywords: zzm321990STKLD1; limb anomaly; nonsense variant; pre-axial polydactyly; serine-threonine kinase
Year: 2019 PMID: 30945277 DOI: 10.1111/cge.13547
Source DB: PubMed Journal: Clin Genet ISSN: 0009-9163 Impact factor: 4.438