Congenital migratory dyskeratosis (Dysmorphism Congenital Migratory) is a hereditary skin disease characterized by the development of symmetrical areas of hyperkeratosis (thickening and keratinization of the skin). In which the following are observed: pronounced disturbances in the formation of hair and nails, gradual weight loss, pallor and atrophy of the skin, their infection (fungal lesions or systemic infection), thickening of the nail plates like “tips”.