Development of a Disease Registry for Autoimmune Bullous Diseases: Initial Analysis of The Pemphigus Vulgaris Subset

33Citations
Citations of this article
55Readers
Mendeley users who have this article in their library.

Abstract

Pemphigus vulgaris (PV) is a rare, potentially life threatening, autoimmune blistering skin disease. The International Pemphigus and Pemphigoid Foundation (IPPF) has recently developed a disease registry with the aim to enhance our understanding of autoimmune bullous diseases with the long-term goal of acquiring information to improve patient care. Patients were recruited to the IPPF disease registry through direct mail, e-mail, advertisements, and articles in the IPPF-quarterly, -website, -Facebook webpage, and IPPF Peer Health Coaches to complete a 38-question survey. We present here the initial analysis of detailed clinical information collected on 393 PV patients. We report previously unrecognized gender differences in terms of lesion location, autoimmune comorbidity, and delay in diagnosis. The IPPF disease registry serves as a useful resource and guide for future clinical investigation.

Cite

CITATION STYLE

APA

Shah, A. A., Seiffert-Sinha, K., Sirois, D., Werth, V. P., Rengarajan, B., Zrnchik, W., … Sinha, A. A. (2015). Development of a Disease Registry for Autoimmune Bullous Diseases: Initial Analysis of The Pemphigus Vulgaris Subset. Acta Dermato-Venereologica, 95(1), 86–90. https://doi.org/10.2340/00015555-1854

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free