Answer:
This pattern of sweat-gland distribution can be explained by X chromosome inactivation
Explanation:
Women are XX and men are XY, to compensate the genetic information (that women do not have twice as much X information as men), one of these two women's X chromosomes is inactive. X-inactivation occurs during the embryonic process and is random. That is, in some cells one of the Xs can be inactivated, and in other cells the other X can be inactivated. Each of these few embryonic cells will lead to more cells, which will have the same inactive X chromosome as it. Then, in the heterozygous females a mosaic pattern may remain, because in each cell there will be an inactive X chromosome. The anhydrotic dysplasia is linked to the X chromosome, heterozygous women will have some areas in the skin in which cells have inactivated the X chromosome that carries the allele that determines they will have the genetic disorder. In other areas of the skin, the cells will have inactivated the X chromosome that carries the allele that determines they do not have the disease.