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Disease Info Card
Dystonia Disorders
Information about Dystonia Disorders: 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 Dystonia Disorders
Most recent studies have shown that Dystonia Disorders shares some biological mechanisms with basal-ganglia-diseases, blepharospasm, chorea, dyskinesia-drug-induced, dyskinetic-syndrome, dystonia-musculorum-deformans, focal-dystonia, generalized-dystonia, globus-hystericus, lingual-facial-buccal-dyskinesia, movement-disorders, muscle-spasticity, myoclonus, nervous-system-disorder, pain, parkinson-disease, secondary-parkinson-disease, spasm, torticollis.
Among the many pathways, these few ones have gauged particular interests from scientists studying Dystonia Disorders, and have been seen in publications frequently: Aging, Brain Development, Cell Death, Cognition, Excretion, Exocytosis, Hypersensitivity, Innervation, Localization, Locomotion, Mastication, Muscle Contraction, Myelination, Pathogenesis, Reflex, Secretion, Sensitization, Sensory Processing, Translation, Transport
Quite a number of genes have been found to play important roles in Dystonia Disorders, such as ATP1A3, CAMP, CSF2, DST, EEF1A2, GCDH, GCH1, LAMC2, LRP2, MCF2L, PANK2, PYCARD, SGCE, TAF1, TH, THAP1, TIMM8A, TOR1A, TYMS. 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.