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Disease Info Card
Paroxysmal Choreoathetosis
Information about Paroxysmal Choreoathetosis: 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 Paroxysmal Choreoathetosis
Most recent studies have shown that Paroxysmal Choreoathetosis shares some biological mechanisms with ataxia, athetosis, benign-neonatal-epilepsy, channelopathies, chorea, choreoathetosis, convulsions, dyskinesia-paroxysmal, dyskinetic-syndrome, dystonia-disorders, epilepsy, involuntary-movements, migraine-disorders, movement-disorders, paroxysmal-dystonia, paroxysmal-nonkinesigenic-dyskinesia, partial-seizure.
Among the many pathways, these few ones have gauged particular interests from scientists studying Paroxysmal Choreoathetosis, and have been seen in publications frequently: Localization, Pathogenesis, Reflex, Response To Anticonvulsant
Quite a number of genes have been found to play important roles in Paroxysmal Choreoathetosis, such as AURKA, CACNA1A, CAMP, CAT, CP, CRAT, GLYAT, KCNA1, OCA2, PEA15, PNKD, PRKD1, PRRT2, SERPINA7, SLC2A1, SLC4A3. 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.
Pathways Related to Paroxysmal Choreoathetosis
This information is being compiled and will come in a future update
| Localization | Pathogenesis | Reflex |
| Response To Anticonvulsant |