X-linked Periventricular Heterotopia

Overview of X-linked Periventricular Heterotopia

Most recent studies have shown that X-linked Periventricular Heterotopia shares some biological mechanisms with brain-diseases, congenital-abnormality, congenital-cerebellar-hypoplasia, dysplasia, ectopic-tissue, epilepsies-partial, epilepsy, hypoplasia, infantile-spasms, lissencephaly, neuronal-migration-disorders, periventricular-nodular-heterotopia, polymicrogyria, severe-mental-retardation, spasm, subcortical-band-heterotopia, tuberous-sclerosis.

Among the many pathways, these few ones have gauged particular interests from scientists studying X-linked Periventricular Heterotopia, and have been seen in publications frequently: Axonogenesis, Blood Vessel Development, Brain Development, Cell Death, Cell Migration, Localization, Neurogenesis, Pathogenesis

Quite a number of genes have been found to play important roles in X-linked Periventricular Heterotopia, such as ARFGEF2, CALB1, CHP1, DCX, ELN, EMX2, FLNA, MB, MTSS1, PAFAH1B1, PLA2G7, POLD4, POLE4, RELN, STS, TPPP, TSC1, TSC2. 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.

X-linked Periventricular Heterotopia Related Genes

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Pathways Related to X-linked Periventricular Heterotopia

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

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