Mutation spectrum of Fork-Head Transcriptional Factor Gene (FOXL2) in Indian Blepharophimosis Ptosis Epicanthus Inversus Syndrome (BPES) patients
- 1Hyderabad Eye Research Foundation, Hyderabad, India
- 2Hyderabad Eye Institute, LV Prasad Eye Institute, Hyderabad, India
- Correspondence to Dr Inderjeet Kaur, Kallam Anji Reddy Molecular Genetics Laboratory, Champalimaud Translational Centre, Brien Holden Eye Research Centre, LV Prasad Eye Institute, Hyderabad 500034, India;
Contributors IK planned, designed and executed the study, analysed the data and wrote the manuscript. AH participated in the collection of samples and laboratory work. SGH, MNN and RM participated in the study design, clinical diagnosis of the subjects included in the study, data analysis and manuscript writing.
- Accepted 15 January 2011
- Published Online First 16 February 2011
Aim The fork-head transcription factor gene (FOXL2) gene has been implicated in Blepharophimosis Ptosis Epicanthus Inversus Syndrome (BPES) type I and type II. The authors aimed to evaluate the involvement of FOXL2 in familial and sporadic cases of BPES in an Indian cohort.
Methods The present cohort comprised clinically well-characterised BPES cases that included six affected families, two sporadic cases and 60 unaffected normal controls. The 5′ untranslated and coding region of FOXL2 was screened by resequencing and confirmed by restriction digestion. Further, genotype–phenotype correlations were done to understand the implications of the observed mutation.
Results Six mutations were observed in eight cases (87.5%). These included a novel deletion (c.860delC), three previously reported duplications (c.663–692dup 30, c.672–701dup30 and c.843–859dup17), a frame shift (c.804dupC) and a homozygous missense mutation (p.E69K). The p.E69k mutation was seen in both heterozygous and homozygous form in a large four-generational family, and disease severity was found to be directly linked to the allelic dosage. Two SNPs (c.501C→T, c.536C→G) were also noted. An unusual coexistence of polycystic ovarian disease (PCOD) with BPES was also seen in one of the families.
Discussion Mutations in the region downstream of the fork-head domain were predominantly responsible for BPES among Indian patients.
Funding Hyderabad Eye Research Foundation, Hyderabad India.
Competing intersets None.
Ethics approval Ethics approval was provided by the Institutional Review Board, LV Prasad Eye Institute, Hyderabad, India.
Provenance and peer review Not commissioned; externally peer reviewed.