“…At present, more than 60 mutations of this gene have been reported, most of them in oriental individuals who suffer from DSH, but it is not possible to establish a clear correlation between the clinical phenotype and the type of mutation of the DSRAD 12–17 gene. Rare spontaneous cases and cases of autosomal recessive type have been described, mainly in the West 2,7 . Even though it was primarily described as a genodermatosis specific to the oriental race, similar conditions have been reported on people of other races 2,7,18,19 .…”