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Disease Info Card
Sotos' Syndrome
Information about Sotos' 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 Sotos' Syndrome
Most recent studies have shown that Sotos' Syndrome shares some biological mechanisms with acromegaly, brain-diseases, congenital-heart-defects, craniofacial-abnormalities, developmental-delay-(disorder), developmental-disabilities, gigantism, growth-disorders, haploinsufficiency, learning-disabilities, learning-disorders, macrocephaly, malignant-neoplasms, neoplasms, nervousness, scoliosis-unspecified, weaver-syndrome.
Among the many pathways, these few ones have gauged particular interests from scientists studying Sotos' Syndrome, and have been seen in publications frequently: Aging, Associative Learning, Bone Development, Bone Maturation, Brain Development, Coagulation, Conditioned Taste Aversion, Feeding Behavior, Histone Modification, Insulin Secretion, Localization, Long-term Memory, Methylation, Ossification, Oxidative Phosphorylation, Pathogenesis, Proteolysis, Secretion, Translation
Quite a number of genes have been found to play important roles in Sotos' Syndrome, such as ABCC8, BBS9, CD19, CREB1, GPC3, IGF1, IGFBP3, INS, MS4A1, NOS1, NSD1, SLC17A5, SPANXB1. 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.