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Disease Info Card
Pfaundler-hurler Syndrome
Information about Pfaundler-hurler 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 Pfaundler-hurler Syndrome
Most recent studies have shown that Pfaundler-hurler Syndrome shares some biological mechanisms with dwarfism, dysostoses, dysplasia, inborn-errors-of-metabolism, lysosomal-storage-diseases, metabolic-diseases, mucolipidoses, mucopolysaccharidoses, mucopolysaccharidosis-i, mucopolysaccharidosis-ii, mucopolysaccharidosis-iii, mucopolysaccharidosis-iv, mucopolysaccharidosis-v, mucopolysaccharidosis-vi, nervousness, retinitis-pigmentosa, storage-disease, type-ii-mucolipidosis.
Among the many pathways, these few ones have gauged particular interests from scientists studying Pfaundler-hurler Syndrome, and have been seen in publications frequently: Aging, Bone Development, Cognition, Elastic Fiber Assembly, Endocytosis, Excretion, Fatty Acid Oxidation, Habituation, Immune Response, Localization, Ossification, Pathogenesis, Pigmentation, Secretion, Sulfation, Tolerance Induction, Tooth Eruption, Translation, Transport, Urea Cycle
Quite a number of genes have been found to play important roles in Pfaundler-hurler Syndrome, such as AGA, ARSA, ARSB, ARSH, CD34, CSF2, CTSA, DHPS, ELF3, ELN, GALNS, GLB1, GUSB, IDUA, LAMC2, MAP3K14, PRPH2. 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.