Factors associated with impaired quality of life and support group utilization in autoimmune bullous disease

J Am Acad Dermatol. 2023 Oct;89(4):813-815. doi: 10.1016/j.jaad.2023.05.062. Epub 2023 Jun 1.

Authors

Samantha Herbert¹, Renee Haughton¹, Kimberly Artounian², Lauren Downing¹, Antonio Ji-Xu³, Emanual Maverakis¹

Affiliations

¹ Department of Dermatology, University of California, Davis, Sacramento, California.
² United Health Services Southern California Medical Education Consortium, Temecula, California.
³ Department of Dermatology, University of California, Davis, Sacramento, California; Oxford University Hospitals NHS Foundation Trust, Oxford, United Kingdom. Electronic address: ajixu@ucdavis.edu.

PMID: 37269926
DOI: 10.1016/j.jaad.2023.05.062

No abstract available

Keywords: blistering disorders; bullous pemphigoid; coping; pemphigus vulgaris; quality of life; support group.

MeSH terms

Autoimmune Diseases*
Humans
Pemphigus*
Quality of Life