Epidermolysis bullosa acquisita: A retrospective analysis of 12 patients evaluated in four tertiary hospitals in Spain

Abstract:

Summary Background Epidermolysis bullosa acquisita is an exceedingly rare subepidermal blistering disease caused by antibodies against type VII collagen. Studies summarizing the clinical and immunological features of this disease in large series of patients are scarce.

Año de publicación:

2014

Keywords:

Fuente:

scopus