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Disease Info Card
Interfrontal Craniofaciosynostosis
Information about Interfrontal Craniofaciosynostosis: characteristics, related genes and pathways, plus antibodies you can use for research. This page is being enriched constantly, if you see some information you would like this page to include please send your suggestions to us.
Overview of Interfrontal Craniofaciosynostosis
Most recent studies have shown that Interfrontal Craniofaciosynostosis shares some biological mechanisms with blood-loss-surgical, congenital-abnormal-synostosis, congenital-abnormality, congenital-heart-defects, craniosynostosis, cytogenetic-abnormality, developmental-delay-(disorder), developmental-disabilities, epilepsy, haploinsufficiency, hemorrhage, hydrocephalus, interparietal-craniosynostosis, microcephaly, pregnancy-complications, scaphycephaly, trigonocephaly, trigonocephaly-syndrome.
Among the many pathways, these few ones have gauged particular interests from scientists studying Interfrontal Craniofaciosynostosis, and have been seen in publications frequently: Cell Growth, Inflammatory Response, Osteoblast Differentiation, Wound Healing
Quite a number of genes have been found to play important roles in Interfrontal Craniofaciosynostosis, such as BMP2, CDKN2A, CDON, CER1, FBN2, FGFR1, FGFR2, FREM1, FUT2, GLI3, MB, NF1, PTCH1, RFC1, RFC2, RUNX2, TINAGL1, TWIST1. See what Boster has to offer for the research of these genes by clicking the gene name links below and view a more detailed info card/product listing for that gene.
In a later update, we will include information such as current drugs and therapy solutions as well as on-going and past clinical trials for this disease. Plesae stay updated.
Pathways Related to Interfrontal Craniofaciosynostosis
This information is being compiled and will come in a future update
| Cell Growth | Inflammatory Response | Osteoblast Differentiation |
| Wound Healing |