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Disease Info Card
Periventricular Nodular Heterotopia
Information about Periventricular Nodular Heterotopia: 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 Periventricular Nodular Heterotopia
Most recent studies have shown that Periventricular Nodular Heterotopia shares some biological mechanisms with brain-diseases, congenital-abnormality, congenital-neurologic-anomalies, cortical-dysplasia, dysplasia, ectopic-tissue, epilepsies-partial, epilepsy, hypoplasia, lissencephaly, malformations-of-cortical-development, neuronal-migration-disorders, paroxysmal-nocturnal-hemoglobinuria, polymicrogyria, schizencephaly, subcortical-band-heterotopia, x-linked-periventricular-heterotopia.
Among the many pathways, these few ones have gauged particular interests from scientists studying Periventricular Nodular Heterotopia, and have been seen in publications frequently: Anaphase, Blood Vessel Development, Brain Development, Cell Adhesion, Cell Cycle, Cell Development, Cell Migration, Central Nervous System Development, Glycosylation, Localization, Long-term Memory, M Phase, Mitosis, Nervous System Development, Neurogenesis, Pathogenesis, Platelet Aggregation, Stem Cell Development, System Development, Transport
Quite a number of genes have been found to play important roles in Periventricular Nodular Heterotopia, such as ARFGEF2, ARX, CALB2, DCX, EMX2, EXOSC10, FLNA, FMR1, MLYCD, PAFAH1B1, PAH, PLA2G7, RELN, SGCG, TSC1, TSC2, TUBA1A, UBA2. 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.