Robinow syndrome can also be caused by mutations in other genes that are important in the WNT/PCP signaling pathway, including WNT5A (OMIM 180700), the disheveled genes DVL1 (OMIM 616331), DVL2, and DVL3 (OMIM 616894), and the WNT co-receptors FZD2 and ROR2 (OMIM 268310) [8, 9]. This evidence concerns the gene WNT5A and Robinow syndrome.