FOXC1 and glaucoma: In present study, we identified a heterozygous variant p.Leu247Gln in a consanguineous family i.e., PCG060 and absence of any other heterozygous/homozygous variant in CYP1B1, recessive inheritance pattern and previously reported allelic interactions of two un linked genes for PCG phenotype [12, 13, 48] necessitates genetic analysis of other glaucoma related genes including MYOC, FOXC1 and TEK genes in PCG060 family.