Epidermolysis bullosa simplex 1D, generalized, intermediate or severe, autosomal recessive

A basal subtype of epidermolysis bullosa simplex EBS characterized by generalized or, less frequently, localized acral blistering.

Also known as: EBS, autosomal recessive K14, EBS-AR KRT14, KRT14-related autosomal recessive EBS, KRT14-related autosomal recessive epidermolysis bullosa simplex, KRT14-related epidermolysis bullosa simplex, epidermolysis bullosa simplex 1D, generalized, intermediate or severe, autosomal recessive, epidermolysis bullosa simplex, autosomal recessive type 1, EBSB1

8 clinical trials for this condition and its sub-types.