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Epidermolysis Bullosa Acquisita - StatPearls - NCBI Bookshelf Epidermolysis bullosa acquisita (EBA) is a rare, chronic autoimmune blistering disease that affects both the skin and mucous membranes This condition arises due to autoantibodies targeting type VII collagen—a crucial component of anchoring fibrils within the dermal-epidermal junction
Epidermolysis bullosa acquisita Epidermolysis bullosa (EB) is the name given to a group of inherited blistering diseases that are present from birth What is epidermolysis bullosa acquisita? Epidermolysis bullosa acquisita (EBA) is a rare autoimmune blistering disease in which tense subepithelial blisters appear at sites of trauma
UpToDate Epidermolysis bullosa acquisita is a rare, chronic skin disorder characterized by fragile skin and blister formation, requiring careful diagnosis and management
Epidermolysis Bullosa Acquisita - PubMed Epidermolysis bullosa acquisita (EBA) is a rare, chronic autoimmune blistering disease that impacts both the skin and mucous membranes This condition arises due to autoantibodies targeting type VII collagen—a crucial component of anchoring fibrils within the dermal-epidermal junction (DEJ)
Epidermolysis bullosa: Overview Epidermolysis bullosa simplex causes blistering in the outermost layer of skin, which is the epidermis EBS can also be more severe Blistering may be widespread and occur anywhere on the skin or inside the mouth The nails can be rough and thick or missing