Dysplasia Ectodermal Congenital Hydrotic

Dysplasia ectrodal congenita hydrota (D.E.C.H) is a rare genetic disease characterized by dysmorphology of the outer integument. The development of dystrophic processes occurs in the epidermis, dermis, connective tissue and other areas of the surface of the skin and mucous membranes. The cause of the disease lies in the mutation of the HPP12-TACN gene, localized in the area