Characteristics of Patients With Recessive Dystrophic Epidermolysis Bullosa
Status: Recruiting
Location: See location...
Study Type: Observational
SUMMARY
Recessive dystrophic epidermolysis bullosa (RDEB) is a disease caused by genetic mutations in the gene for type VII collagen. Patients with RDEB develop large, severely painful blisters and open wounds from minor trauma to their skin. We are screening subjects with RDEB to evaluate characteristics of the subjects and their cells in order to develop new strategies of therapy and determine whether subjects could be candidates for treatment studies.
Eligibility
Participation Requirements
Sex: All
Healthy Volunteers: f
View:
• Clinical diagnosis of RDEB by local dermatologist
• 7 years of age or older
Locations
United States
California
Stanford University School of Medicine
RECRUITING
Stanford
Contact Information
Primary
Irene Bailey-Healy
baileyhi@stanford.edu
(650) 721-7149
Time Frame
Start Date: 2009-11-10
Estimated Completion Date: 2029-12-31
Participants
Target number of participants: 70
Authors
Marius Wernig, Paul A. Khavari
Related Therapeutic Areas
Sponsors
Leads: Stanford University