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Disease Info Card
Mobius Syndrome
Information about Mobius 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 Mobius Syndrome
Most recent studies have shown that Mobius Syndrome shares some biological mechanisms with abducens-nerve-diseases, autistic-disorder, congenital-abnormality, congenital-disorders, cranial-nerve-diseases, diplegia, duane-retraction-syndrome, facial-nerve-diseases, facial-paralysis, facial-paresis, hypoplasia, limb-deformities-congenital, micrognathism, nerve-paralysis, ophthalmoplegia, paresis, poland-syndrome, strabismus, weakness.
Among the many pathways, these few ones have gauged particular interests from scientists studying Mobius Syndrome, and have been seen in publications frequently: Bone Maturation, Cognition, Cranial Nerve Development, Developmental Process, Fertilization, Habituation, Immune Response, Innervation, Localization, Mastication, Nerve Development, Ossification, Pathogenesis, Reflex, Regeneration, System Development, Transposition, Vasculogenesis, Vasoconstriction, Wound Healing
Quite a number of genes have been found to play important roles in Mobius Syndrome, such as BCHE, CD82, CELA3B, CHP1, DCTN3, FGF8, FGF9, IFT122, KIF21A, PHOX2A, PLXND1, POMC, SOX14, SS18L1. 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.