Jun 12, 2024 · Learn about a rare inherited disease that often shows up in infancy and causes fragile, blistering skin on the palms and feet. Severe disease may be fatal.

Epidermolysis bullosa dystrophica or dystrophic EB (DEB) is an inherited disease affecting the skin and other organs. [1] [2] "Butterfly child" is the colloquial name for children born with the disease, as their skin is seen to be as delicate and fragile as the wings of a butterfly. [3]

Epidermolysis bullosa is a connective tissue disorder that causes your skin to blister and tear easily. Treatment helps prevent blisters from forming, care for blisters and skin, treat nutritional problems that arise from blisters in the mouth or esophagus and manage pain.

Epidermolysis bullosa (EB) is a group of rare medical conditions that result in easy blistering of the skin and mucous membranes. Blisters occur with minor trauma or friction and are painful. Its severity can range from mild to fatal. [7] . Inherited EB is a rare disease with a prevalence in the United States of 8.2 per million live births. [8] .

Dystrophic epidermolysis bullosa is one of the major forms of a group of conditions called epidermolysis bullosa. Epidermolysis bullosa cause the skin to be very fragile and to blister easily. Blisters and skin erosions form in response to minor injury or …

Dystrophic epidermolysis bullosa (DEB): When a child has a mild case of DEB, blisters tends to develop only on the hands, feet, knees, and elbows. Blistering can also be widespread, causing severe DEB. A baby born with severe DEB, can have …

Aug 21, 2006 · Dystrophic epidermolysis bullosa (DEB) is a genetic skin disorder affecting skin and nails that usually presents at birth. DEB is divided into two major types depending on inheritance pattern: recessive dystrophic epidermolysis bullosa (RDEB) and dominant dystrophic epidermolysis bullosa (DDEB).

debra of America is a national nonprofit organization dedicated to improving the lives of people with Epidermolysis Bullosa (EB) through supportive programs and funding the most innovative research for treatments and a cure. Explore further to learn how we help those with EB and their families and how you can get involved in our mission.

Epidermolysis Bullosa, or EB, is a group of rare disorders caused by a mutation in one of 18 genes. There are four major types: Simplex, Junctional, Dystrophic, and Kindler, and the specific type of EB is determined by the affected gene.

Dystrophic epidermolysis bullosa (DEB) is one of the major forms of epidermolysis bullosa. The signs and symptoms can vary widely among affected people. In mild cases, blistering may primarily affect the hands, feet, knees, and elbows.