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Disease Info Card
Motor Apraxia
Information about Motor Apraxia: 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 Motor Apraxia
Most recent studies have shown that Motor Apraxia shares some biological mechanisms with aphasia, apraxia-ideomotor, apraxias, ataxia, ataxia-telangiectasia, atrophy, cerebellar-ataxia, comatose, dystonia-disorders, hypoplasia, movement-disorders, muscle-hypotonia, nervousness, nystagmus, ocular-motility-disorders, oculomotor-apraxia, ophthalmoplegia, spinocerebellar-degeneration, telangiectasis.
Among the many pathways, these few ones have gauged particular interests from scientists studying Motor Apraxia, and have been seen in publications frequently: Aging, Cell Adhesion, Cell Death, Cognition, Dna Ligation, Dna Repair, Excretion, Innervation, Localization, Locomotion, Myelination, Pathogenesis, Reflex, Visual Perception
Quite a number of genes have been found to play important roles in Motor Apraxia, such as ADSL, AFP, ALB, APTX, DCX, FXN, GRN, NPHP1, NPHP4, NXPH1, PARP1, POLB, PRNP, SETX, SSB, XRCC1. 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 Motor Apraxia
This information is being compiled and will come in a future update
| Aging | Cell Adhesion | Cell Death |
| Cognition | Dna Ligation | Dna Repair |
| Excretion | Innervation | Localization |
| Locomotion | Myelination | Pathogenesis |
| Reflex | Visual Perception |