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Disease Info Card
Acrocephalosyndactylia
Information about Acrocephalosyndactylia: 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 Acrocephalosyndactylia
Most recent studies have shown that Acrocephalosyndactylia shares some biological mechanisms with acrocephaly, airway-obstruction, apert-syndrome, cleft-palate, congenital-abnormal-synostosis, congenital-abnormality, congenital-hand-deformities, craniofacial-dysostosis, craniosynostosis, dysostoses, exophthalmos, hydrocephalus, hypoplasia, malocclusion, orbital-separation-excessive, pfeiffer-syndrome, saethre-chotzen-syndrome, stenosis, syndactyly.
Among the many pathways, these few ones have gauged particular interests from scientists studying Acrocephalosyndactylia, and have been seen in publications frequently: Aging, Bone Development, Cell Adhesion, Cell Growth, Cell Migration, Cell Proliferation, Endochondral Ossification, Limb Development, Limb Morphogenesis, Localization, Ossification, Osteoblast Differentiation, Osteoblast Proliferation, Pathogenesis, Secretion, Segmentation, Tooth Eruption, Translation, Transport, Transposition
Quite a number of genes have been found to play important roles in Acrocephalosyndactylia, such as ACCS, ACSS2, BGLAP, FGF10, FGF13, FGF2, FGFR1, FGFR2, FGFR3, FUT3, GLI3, HPS4, MAPK1, MAPK3, MSX2, PLA2G15, RUNX2, SPP1, 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.