epidermolyysiä

Epidermolysis is a group of rare genetic disorders that cause the skin to be extremely fragile. The slightest friction or trauma can cause blisters and sores to form on the skin. The severity of epidermolysis varies greatly depending on the specific type of the condition. In mild cases, blisters may only occur on the hands and feet. In severe cases, blisters can occur anywhere on the body, including the inside of the mouth and digestive tract.

The underlying cause of epidermolysis is a genetic mutation that affects the proteins responsible for anchoring the different layers of the skin together. When these proteins are faulty, the skin layers separate easily, leading to blistering. There are several different subtypes of epidermolysis, each caused by mutations in different genes.

There is currently no cure for epidermolysis. Treatment focuses on managing symptoms, preventing infection, and promoting wound healing. This often involves careful wound care, pain management, and supportive therapies. Individuals with epidermolysis require lifelong management and often a multidisciplinary approach to care involving dermatologists, geneticists, and other specialists. The condition can have significant impacts on a person's quality of life, affecting mobility, nutrition, and social interactions.