In our study, 3 patients were diagnosed with dystrophic epidermolysis bullosa (DEB) with mutations in the collagen VII alpha-1 polypeptide gene and 1 patient had an epidermolysis bullosa simplex (EBS), Dowling-Meara type, with a mutation in the keratin 14 gene. Here, KRT14 is linked to Dystrophic epidermolysis bullosa.