Epidermolysis bullosa acquisita, Brunsting-Perry type (Q85876): Difference between revisions

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Latest revision as of 11:14, 15 August 2026

The Brunsting-Perry variant of epidermolysis bullosa acquisita is a rare mechanobullous autoimmune skin disease characterised by blistering and scarring of facial or scalp skin and the presence of IgG autoantibodies to the basement membrane anchoring fibril, collagen VII. This distinguishes it from the clinically similar Brunsting-Perry variant of cictricial pemphigoid in which this antibody is not found.

Language	Label	Description	Also known as
default for all languages	ID_1417911502
English	Epidermolysis bullosa acquisita, Brunsting-Perry type	The Brunsting-Perry variant of epidermolysis bullosa acquisita is a rare mechanobullous autoimmune skin disease characterised by blistering and scarring of facial or scalp skin and the presence of IgG autoantibodies to the basement membrane anchoring fibril, collagen VII. This distinguishes it from the clinically similar Brunsting-Perry variant of cictricial pemphigoid in which this antibody is not found.