Three of the four missense TERT gene mutations, T726M, A1062T, and V1090M, within our sample cohort were previously described by Liang et al. [26], Calado et al. [13], Calado et al. [25], and Yamaguchi et al. [16], in patients with other telomere diseases: severe aplastic anemia, acute myeloid leukemia, and cirrhosis. This evidence concerns the gene TERT and idiopathic aplastic anemia.