Mutations in FOXL2 underlying BPES (types 1 and 2) in Colombian families

Publisher Website
Google Scholar
Abstract
We report the genetic characterization of one family with blepharophimosis‐ptosis‐epicanthus inversus syndrome (BPES) type 1 and two families with BPES type 2 from a historically isolated population in northwest Colombia. Linkage and haplotype analyses indicate that BPES in these families is linked to 3q23. Mutation screening of FOXL2 in the family with BPES type 1 revealed a novel 394C → T nonsense mutation which deletes the forkhead DNA binding domain. The two families with BPES type 2 both carry an in‐frame 30 bp duplication that leads to the elongation of a polyalanine tract. This duplication has been previously reported in Europe, where recurrent mutation has been demonstrated in unrelated familial and sporadic BPES cases. The recurrent nature of this duplication seems to relate to the secondary structure of this DNA region. The genotype–phenotype correlation seen in the Colombian families is consistent with the recent proposal that BPES type 1 is caused by truncating mutations leading to haploinsufficiency, while BPES type 2 is due to mutations generating elongated protein products.
Funding Information
  • CODI (CPT-9901)
  • Colciencias (CIM-2140)