What are the most fierce skin diseases?

Rare skin diseases are often limited to isolated parts of the world's population. Many doctors, including dermatologists who specialize in skin handling, can spend their entire career that has never met with the only example of hundreds of rare skin diseases that exist. This is due to the fact that they usually occur only in a handful of people for every million people in the human population. These diseases include the recessive dystrophic epidermolysis Bullosa (Rdeb), tinea imbricata or tokelau ringworm, found only in the Mindanao tribe in the Philippines, and Stevens-Johnson Syndrome), which occurs as an unfavorable response to a million. Rare skin disorders may have genetic, environmental or unknown causes, and although many have no known treatment, some are easy to treat as soon as it is identified. Some infection. Causes skin lesions and other adverse effects such as loss of memory and pain of clotUbů, and was identified in about 2,000 to 4,500 people in the American population of 307,000,000 since 2011. Like several rare skin diseases, there is no known medicine for Morgellon, which first identified in 2001 Mary Leitao that he was in Pennsylvania.

In the Mindanao tribe in the province of Sarangani in the Philippines, tinea imbricata is caused by the fungal infection of Tokelau. It creates a kind of scaly, formula of peeling of the skin similar to the fingerprint, which can spread to large parts of the body, but responds to conventional treatment when identified. Since 1990, only three cases of disease have been reported around the world, one of which stretched until 1789. In Leaod 2011 it was found that the individuals of ST 28 were infected with disease and all new cases were in the Mindanao tribe.

Rdeb was an example among rare genetic diseases incurable until 2010, when it was treated in the US10 children with stem cells obtained from bone marrow. RDEB diseases were diagnosed as in approximately 20 newborns in the United States for every 1,000,000 live births and international efforts from the US, Great Britain and Japan have been working on treatment and possible medicines since 2010. Like many rare skin diseases, RDEBs primarily affect children, because its results can be so serious that they usually lead to premature death. Thanks to this disease, the skin is very sensitive to friction, causing blistering and scratching, and this effect also occurs inner skin surfaces such as the mouth and esophagus, which can lead to extreme pain for basic activities such as eating.