“…It has also boost up or affected by deficient enzymes or transport proteins that are essential for lipid metabolism in the epidermis (cholesterol sulphatase, lipoxygenases, ABCA12, etc.). Mutations in epidermal keratins cause several skin diseases like congenital ichthyosis, epidermolytic ichthyosis, congenital bullous disease, corneal dystrophy, erythroderma, and pachyonychia congenital [74][75][76]. All the above diseases are due to mutation in the corneal keratin genes (KRT3, KRT12); mutation in simple epithelial keratin genes (KRT8/18, KRT19, KRT9); mutations in epithelial keratin genes (KRT6A, KRT6B, KRT6C, KRT16 or KRT17); mutations inKRT1 or KRT10 or basal layer keratinocytes genes (KRT5&KRT14) [77,78].…”