KRT14-related epidermolysis bullosa simplex (Orphanet_89838) can be described as follows. Autosomal recessive epidermolysis bullosa simplex (EBS-AR) is a basal subtype of epidermolysis bullosa simplex EBS (see this term) characterized by generalized or, less frequently, localized acral blistering. Also known as: EBS-AR KRT14.