SETBP1 and Schnyder corneal dystrophy: As observed in Figure 2, of the S. aureus isolates obtained from the patients with SCD, the current study confirmed the finbA gene carriage in 97.9% (N = 46), and the sdrC, sea, tst, clfA, coa, spa, finbB, agr, nuc, efb, pvl, sdrD, hlg, hla, seb, sec, sed, and icaA genes were demonstrated in 100% (N = 47), 25.5% (N = 12), 4.3% (N = 2), 97.9% (N = 46), 100% (N = 47), 42.6% (N = 20), 100% (N = 47), 46.8% (N = 22), 100% (N = 47), 97.9% (N = 46), 54.3% (N = 25), 100% (N = 47), 100% (N = 47), 100% (N = 47), 27.7% (N = 13), 12.8% (N = 6), 4.3% (N = 2), and 100% (N = 47), respectively.