Disease Info Card

Pfeiffer Syndrome

Information about Pfeiffer Syndrome: 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 Pfeiffer Syndrome

Most recent studies have shown that Pfeiffer Syndrome shares some biological mechanisms with achondroplasia, acrocephalosyndactylia, airway-obstruction, ankylosis, apert-syndrome, congenital-abnormal-synostosis, congenital-abnormality, craniofacial-dysostosis, craniosynostosis, dysostoses, dysplasia, exophthalmos, hydrocephalus, hypoplasia, intracranial-hypertension, orbital-separation-excessive, saethre-chotzen-syndrome, stenosis, syndactyly, thanatophoric-dysplasia.

Among the many pathways, these few ones have gauged particular interests from scientists studying Pfeiffer Syndrome, and have been seen in publications frequently: Angiogenesis, Bone Remodeling, Cell Division, Cell Growth, Cell Proliferation, Flight, Localization, Oncogenesis, Ossification, Osteoblast Differentiation, Osteoblast Proliferation, Pathogenesis, Rna Splicing, Wound Healing

Quite a number of genes have been found to play important roles in Pfeiffer Syndrome, such as CSF2, FGF10, FGF13, FGF2, FGF8, FGFR1, FGFR2, FGFR3, FUT3, HPS4, LAMC2, MAPK1, MAPK3, MSX2, PLA2G15, RUNX2, SLC25A5, 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.