Coronal craniosynostosis is found in humans with mutation genes encoding for MSX2 (Boston type craniosynostosis), TWIST and TCF12 (Saethre-Chotzen syndrome), as well as FGFR3 (Muenke craniosynostosis)41, which could be interesting candidate genes for further investigations of a possible underlying genetic defect in peke-face Persians. The gene discussed is MSX2; the disease is Craniosynostosis, Boston type.