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Disease Info Card
Lesch-nyhan Syndrome
Information about Lesch-nyhan 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 Lesch-nyhan Syndrome
Most recent studies have shown that Lesch-nyhan Syndrome shares some biological mechanisms with athetosis, chorea, choreoathetosis, dystonia-disorders, genetic-diseases-inborn, gout, hereditary-diseases, hyperuricemia, inborn-errors-of-metabolism, kidney-calculi, kidney-diseases, kidney-failure, metabolic-diseases, muscle-spasticity, nervous-system-disorder, nervousness, purine-metabolism-disorder.
Among the many pathways, these few ones have gauged particular interests from scientists studying Lesch-nyhan Syndrome, and have been seen in publications frequently: Adenosine Transport, Brain Development, Cell Growth, Cognition, Dna Repair, Dopamine Uptake, Excretion, Fertilization, Hypersensitivity, Localization, Metaphase, Methylation, Neurogenesis, Pathogenesis, Rna Splicing, Senescence, Sensitization, Translation, Transport
Quite a number of genes have been found to play important roles in Lesch-nyhan Syndrome, such as ADA, APRT, BBS9, BRAP, CAT, EIF3B, G6PD, HPRT1, IMPA1, LMOD1, PNP, PPAT, PPY, QPCT, XDH. 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.