Paroxysmal Dystonia

Overview of Paroxysmal Dystonia

Most recent studies have shown that Paroxysmal Dystonia shares some biological mechanisms with athetosis, chorea, choreoathetosis, dyskinesia-paroxysmal, dyskinetic-syndrome, dystonia-disorders, dystonia-primary, epilepsy, epilepsy-frontal-lobe, generalized-dystonia, involuntary-movements, movement-disorders, multiple-sclerosis, nervous-system-disorder, nocturnal-paroxysmal-dystonia, paroxysmal-nonkinesigenic-dyskinesia, sclerosis, sleep-disorders.

Among the many pathways, these few ones have gauged particular interests from scientists studying Paroxysmal Dystonia, and have been seen in publications frequently: Brain Development, Dopamine Uptake, Hypersensitivity, Localization, Pathogenesis, Reflex, Regeneration, Response To Stress, Synaptic Transmission, Transport

Quite a number of genes have been found to play important roles in Paroxysmal Dystonia, such as AMY2A, ATP1A3, BBS9, BLOC1S6, CAMP, EPB42, GCH1, LRP2, MCF2L, PNKD, PRH1, PRRT2, RNF130, SCN2A, SLC2A1, TH, THAP1, TOR1A. 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.

Paroxysmal Dystonia Related Genes

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Pathways Related to Paroxysmal Dystonia

This information is being compiled and will come in a future update

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