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Disease Info Card
Focal Dystonia
Information about Focal Dystonia: 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 Focal Dystonia
Most recent studies have shown that Focal Dystonia shares some biological mechanisms with blepharospasm, dystonia-disorders, dystonia-musculorum-deformans, dystonia-primary, generalized-dystonia, meige-syndrome, movement-disorders, muscle-cramp, muscle-spasticity, organic-writers-cramp, pain, parkinson-disease, secondary-parkinson-disease, spasm, spasmodic-dysphonia, spasmodic-torticollis, torticollis.
Among the many pathways, these few ones have gauged particular interests from scientists studying Focal Dystonia, and have been seen in publications frequently: Associative Learning, Collateral Sprouting, Dedifferentiation, Exocytosis, Habituation, Hypersensitivity, Innervation, Localization, Mastication, Muscle Contraction, Muscle Hypertrophy, Pathogenesis, Prepulse Inhibition, Proprioception, Reflex, Sensitization, Sensory Processing, Swimming, Transport
Quite a number of genes have been found to play important roles in Focal Dystonia, such as BTN1A1, CAMP, CD82, CP, DIO2, GCH1, GRIP1, LRP2, MCF2L, PMEL, PRPS1, PYCARD, SI, SLC4A7, 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.