A Life-Threatening Disease Causing Infants to Blister, Epidermolysis Bullosa

The symptoms of this disease are mainly revealed by blisters formed by the baby. There are various variations in symptoms. Sometimes blisters are calm and can only appear on the skin. If this happens, blisters are not terrible. People in this state need to avoid rough clothing and keep the skin moist. A possible problem that can occur when blisters occur is to avoid infection by blisters. When blisters are infected, it is easy to distinguish. If the blisters have pus or heat, the best way is to drink antibiotics to suppress the growth of bacteria.

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. Hypoplasia This is the term introduced by Virchow in 1870, from Greek "under" and plastis / plasein "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.

Hassan was born in a rare hereditary skin disorder called bullous epidermal desquamation, causing skin fragility and blister formation. His first blister appeared at the age of 1, but the situation got worse immediately after his family had escaped from their hometown of Syria and arrived in Germany as a refugee. By June 2015, Hassan was hospitalized for a seriously ill patient and almost lost skin on the whole body surface. "Apart from his face, hands, and feet, he did not leave my skin," his father remembered. Amazing scientific progress, the De Luca team continued to develop a complete alternative skin replacing Hassan. Several months after dressing from head to toe, Hassan appeared to cure his devastating illness. Two years has passed, he is very good, his skin no longer blisters, he does not need medicine or ointment, he heals normally when he gets an incision