Show pageBacklinksCite current pageExport to PDFBack to top This page is read only. You can view the source, but not change it. Ask your administrator if you think this is wrong. ====== Syndromic Craniosynostosis Etiology ====== In terms of syndromic craniosynostosis not only do [[Fibroblast growth factor receptor 3]] and [[TWIST transcription factor]] feature, but also [[FGFR1]] and in particular [[FGFR2]], which has been reported in 90% of the syndromic craniosynostoses such as Apert, Crouzon, Peiffer and Jackson–Weiss. The mutations can be divided into mutations that lead to gain of function (in FGFR genes) and mutations that lead to loss of function (in TWIST genes). syndromic_craniosynostosis_etiology.txt Last modified: 2024/06/07 02:58by 127.0.0.1