Characteristics of Adult Patients With Recessive Dystrophic Epidermolysis Bullosa

Stanford University

Status: Completed

Conditions: Epidermolysis Bullosa Dystrophica

Study type: Observational

Funder types: Other

Identifiers

NCT00904163

SU-04232009-2383

Details and patient eligibility

About

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.

Enrollment: 13 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:1. Clinical diagnosis of RDEB by local dermatologist. 2. 18 years of age or more and willing to give consent. Exclusion Criteria:1. Medical instability limiting ability to travel to Stanford University Medical Center.