Bullous epidermolysis is also known as E. coli. It is usually hereditary connective tissue disease. This disease may occur at birth or in the near future. It causes blisters filled with much moisture on the skin and mucous membranes. Even at high temperatures at room temperature, these blisters can form. E, B estimate that 50 out of 1 million live births are affected. As we all know, this disease affects all races and countries, and there are men and women all over the world. Various forms of diseases have been found, from mild to lethal form including several organs.
Bullous epidermolysis syndrome Bullous epidermolysis is an inherited connective tissue disease that causes blisters on the skin and mucosa with an incidence of 1 / 50,000. This is the result of an imperfect fixation between the dermis and the epidermis, resulting in friction and fragility of the skin. Its severity ranges from mild to fatal. Low Formation This is the term introduced by Virchow in 1870 from "Greek" under "and Plus / Plessin" Formation / Formation ". This means that the development of tissues or organs is stagnant or insufficient. Although the majority of the cause of dysplasia is a hereditary disorder, it can also be caused by toxicological phenomena (eg exposure of intrauterine embryos to specific chemicals or teratogenic drugs).
Because he was suffering from a hereditary disease, the skin became too fragile to survive and was sent to Roua University Children's Hospital in 2015. This disease is known as bullous epidermolysis bullosa. As a result, slight friction (such as mild friction) may cause the skin to blister, crack, or fall off. After contacting, De Luca flew and received treatment, but before that he received treatment only twice and received treatment in only a small part of the body. Although this treatment which has little history in the real world is clearly not approved for general use, in many countries, in order to acknowledge such treatment under severe use conditions, an exception of "sympathy for use" there is.