Munier et al. recognized the relationships between TGFBI mutations and specific corneal dystrophies [1]: p.Arg124Leu is found in Reis-Bücklers corneal dystrophy (RBCD), p.Arg555Gln leads to Thiel-Behnke corneal dystrophy (TBCD), p.Arg124Cys causes lattice corneal dystrophy type 1 (LCD1), p.Arg555Trp results in granular corneal dystrophy type 1 (GCD1), and p.Arg124His occurs in granular corneal dystrophy type 2 (GCD2) [1]. The gene discussed is TGFBI; the disease is granular corneal dystrophy type II.