Study Status: Completed
Recruit Status: Completed
Study Type: Observational
Official Title: Characteristics of Adult Patients With Recessive Dystrophic Epidermolysis Bullosa
Brief Summary: Recessive dystrophic epidermolysis bullosa (RDEB) is a severe inherited blistering disease caused by the absence of type VII collagen. Patients with RDEB develop large, severely painful blisters and open wounds from minor trauma to their skin. We are screening RDEB subjects to determine additional characteristics of patients who survive to adulthood.