A Case of Ophiasis Type of Alopecia Areata in a Patient with Ring Chromosome 18 Syndrome

    June 2014 in “ The Journal of Dermatology ”
    Yoshiko Kagimoto, Masato Mizuashi, Katsuko Kikuchi, Setsuya Aiba
    Studysummary This article describes a case of a patient with both ophiasis-type alopecia areata and ring chromosome 18 syndrome but reports no new research findings.
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    Research cited in this study 2

    1. APCDD1 Is a Novel Wnt Inhibitor Mutated in Hereditary Hypotrichosis Simplex Nature · 2010
    2. Genomewide Scan for Linkage Reveals Evidence of Several Susceptibility Loci for Alopecia Areata The American Journal of Human Genetics · 2007