Background: Alopecia Areata (AA) is a common inflammatory immune-mediated non-scarring hair loss; however, the exact genetic susceptibility remains to be clarified. Cytotoxic T-lymphocyte Associated Protein 4 (CTLA4) has emerged as a central and critically important modulator of immune responses and is believed to play a crucial rule in AA pathogenesis.
Objectives: To investigate the association of variant (rs231775) within codon 17 with AA risk and outcomes.
Alopecia areata (AA) is a non-scarring hair loss of autoimmune etiology. The autoimmune regulator () gene is believed to be an important driver in AA pathogenesis. Genetic variants can alter mRNA expression levels which may provoke an autoimmune response.
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