FERMT1 and Kindler syndrome: RM has since been documented in EBS, JEB generalized intermediate, RDEB, DDEB, and Kindler syndrome, implicating COL17A1, KRT14, LAMB3, COL7A1, and FERMT1 genes [15,16,17,18,19,20,21,22,23,24,25,26,27,28] (Figure 2, Table 1), and the topic of prior reviews [19,29,30].