FBN1 and Weill-Marchesani syndrome: A clinically indistinguishable autosomal dominant form of WMS is caused by mutations in the fibrillin-1 gene (FBN1) (Faivre et al., 2003a; Faivre et al., 2003b; Sengle et al., 2012), suggesting overlapping function of ADAMTS10 and FBN1 proteins (Apte, 2009; Karoulias et al., 2020b).