SOX10 and Waardenburg syndrome: Genetic variants within SOX2 are associated with anophthalmia and neural alterations [12,13], SOX3 with altered pituitary development [14], SOX10 with Waardenburg syndrome and Hirschsprung’s disease [15], SOX11 with Coffin–Siris syndrome [16], and SOX18 with Hypotrichosis–Lymphedema–Telangiectasia Syndrome (HLTRS) [17].