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Disease Info Card
Laurence-moon Syndrome
Information about Laurence-moon 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 Laurence-moon Syndrome
Most recent studies have shown that Laurence-moon Syndrome shares some biological mechanisms with bardet-biedl-syndrome, blind-vision, diabetes-mellitus, disorder-of-eye, dwarfism, dystrophy, endocrine-system-diseases, hypogonadism, hypothalamic-diseases, kidney-diseases, kidney-failure, kidney-failure-chronic, obesity, polydactyly, retinal-degeneration, retinal-diseases, retinal-dystrophies, retinitis-pigmentosa.
Among the many pathways, these few ones have gauged particular interests from scientists studying Laurence-moon Syndrome, and have been seen in publications frequently: Brain Development, Cation Transport, Cell Proliferation, Excretion, Glomerular Filtration, Localization, Oogenesis, Pathogenesis, Pigmentation, Response To Gonadotropin-releasing Hormone, Secretion, Senescence, Spermatogenesis, Testosterone Secretion, Transport
Quite a number of genes have been found to play important roles in Laurence-moon Syndrome, such as BBS1, BBS2, BRD2, ERG, GGH, GH1, INS, KCNH2, MYO9A, PLOD1, POMC, PRL, RAPGEF5, RCVRN, RPGR, TRH. 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.