Dystrophic bullous epidermolysis in a newborn

Abstract

Congenital bullous epidermolysis is a severe hereditary disease, the main manifestation of which is bubbles that occur after minor mechanical action on the skin and mucous membranes due to congenital violation of the coding of dermo-epidermal proteins. The difficulty in making a diagnosis of congenital bullous epidermolysis is associated with the rarity of pathology and a small number of scientific publications.