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Disease Info Card
Alternating Hemiplegia Of Childhood
Information about Alternating Hemiplegia Of Childhood: 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 Alternating Hemiplegia Of Childhood
Most recent studies have shown that Alternating Hemiplegia Of Childhood shares some biological mechanisms with ataxia, choreoathetosis, developmental-delay-(disorder), dystonia-disorders, epilepsy, headache, hemiparesis, hemiplegia, migraine-disorders, movement-disorders, moyamoya-disease, nervous-system-disorder, nystagmus, ocular-motility-disorders, quadriplegia, weakness.
Among the many pathways, these few ones have gauged particular interests from scientists studying Alternating Hemiplegia Of Childhood, and have been seen in publications frequently: Cell Proliferation, Coagulation, Excretion, Locomotion, Muscle Cell Proliferation, Pathogenesis, Reflex, Secretion, Smooth Muscle Cell Proliferation
Quite a number of genes have been found to play important roles in Alternating Hemiplegia Of Childhood, such as ABR, ATP1A2, ATP1A3, AURKA, CACNA1A, CALCA, DNMT3B, GH1, GSTP1, ICA, LAMC2, MMEL1, MMP9, NR0B1, PLXNB1, SLC1A3, SLC2A1, TIMP1. 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 Alternating Hemiplegia Of Childhood
This information is being compiled and will come in a future update
| Cell Proliferation | Coagulation | Excretion |
| Locomotion | Muscle Cell Proliferation | Pathogenesis |
| Reflex | Secretion | Smooth Muscle Cell Proliferation |