The classic human craniosynostosis syndromes and associated genetic mutations involving coronal suture fusion include Pfeiffer and Jackson–Weiss syndromes (FGFR1) [123,124,125]; Pfeiffer, Apert, Crouzon, Jackson-Weiss, and Beare-Stevenson syndromes (FGFR2) [126,127,128,129,130,131]; Muenke syndrome (FGFR3) [132,133]; Saethre-Chotzen syndrome (TWIST1) [134,135]; craniofrontonasal syndrome (EFNB1) [136,137]; and, Boston-type craniosynostosis syndrome (MSX2) [138,139,140]. The gene discussed is MSX2; the disease is craniofrontonasal syndrome.