Description
EB, or Epidermolysis Bullosa, is a rare genetic skin disorder characterized by extreme fragility of the skin and mucous membranes, leading to blister formation with minimal friction or trauma. The condition is caused by mutations in genes responsible for the structure and cohesion of the skin layers, and it can vary in severity, impacting the patient’s quality of life significantly. Treatment focuses on wound care and managing symptoms, as there is currently no cure.
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