Secondary Dystonia

Overview of Secondary Dystonia

Most recent studies have shown that Secondary Dystonia shares some biological mechanisms with cerebral-palsy, dyskinetic-syndrome, dystonia-disorders, dystonia-musculorum-deformans, dystonia-primary, focal-dystonia, generalized-dystonia, globus-hystericus, involuntary-movements, lingual-facial-buccal-dyskinesia, movement-disorders, muscle-spasticity, myoclonus, nerve-degeneration, pain, parkinson-disease, torticollis.

Among the many pathways, these few ones have gauged particular interests from scientists studying Secondary Dystonia, and have been seen in publications frequently: Brain Development, Cell Cycle, Cognition, Exogen, Localization, Locomotion, Mastication, Muscle Contraction, Pathogenesis, Proprioception, Reflex, Sensory Processing

Quite a number of genes have been found to play important roles in Secondary Dystonia, such as ATP1A3, CAMP, EEF1A2, GCDH, GCH1, LAMC2, LRP2, MAOB, MCF2L, PANK2, PYCARD, RANGAP1, REST, SGCE, SLC17A5, TAF1, THAP1, TOR1A, TYMS, VIM. 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.

Secondary Dystonia Related Genes

click to see detail information for each gene

Pathways Related to Secondary Dystonia

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

Related Diseases