Epidermolysis bullosa (EB) is a rare genetic condition characterized by fragile skin that blisters and forms painful wounds in response to minor injury or damage. It is caused by a problem in the proteins that help hold the layers of the skin together. There are several types of EB, ranging from mild to severe, depending on the specific genetic issue and its impact on the skin. Symptoms may include blisters, open wounds, scarring, and thickened skin. Treatment focuses on managing symptoms and preventing complications, such as keeping the skin clean, applying protective bandages, and using pain management techniques. There is currently no cure for EB, but ongoing research is examining potential treatments and methods to improve quality of life for affected individuals.

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