WNT5A and Robinow syndrome: For example, the craniofacial phenotype of individuals with WNT5A-associated Robinow syndrome include midface hypoplasia, hypertelorism, macrocephaly, short hard palate, micrognathia, cleft lip/palate, and others, but not all pathogenic variants in WNT5A result in the same set of craniofacial anomalies (Conlon et al. 2021; White et al. 2018).