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ABSTRACT: Background
Alopecia areata (AA) is considered complex genetic and tissue-specific autoimmune disease. We recently discovered a nonsynonymous variant in the coiled-coil alpha-helical rod protein 1 (CCHCR1) gene within the AA risk haplotype. And a water avoidance stress test on CCHCR1 knockout mice induced AA-like lesions.Objective
To investigate the difference clinical findings of AA in patients with the CCHCR1 variant and without.Methods
We conducted a retrospective analysis of the data from 142 AA patients. Among these patients, 20 (14.1%) had a variant of CCHCR1. We evaluated the sex distribution of the patients, age at onset, distribution of the clinical types, prevalence of a positive family history of AA, prevalence of association of
SUBMITTER: Koyama S
PROVIDER: S-EPMC10579570 | biostudies-literature | 2023 Oct
REPOSITORIES: biostudies-literature