“…Loose anagen syndrome is attributed to an autosomal dominant or sporadic mutation in the gene encoding keratin 6 [2,3]. One mutation in K6HF, the companion layer keratin which represents the innermost layer of the outer root sheath, prematurely keratinizes the inner root sheath which impairs adhesion between the inner root sheath cuticle and the hair shaft cuticle [1,5,6]. An additional mutation in K6IRS, which is specific to the inner root sheath, impairs adhesion between the inner and outer root sheaths and prematurely terminates anagen [6].…”