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Disease Info Card
Language Delays
Information about Language Delays: 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 Language Delays
Most recent studies have shown that Language Delays shares some biological mechanisms with autism-spectrum-disorders, autistic-disorder, child-development-disorders-pervasive, cognition-disorders, delayed-articulatory-and-language-development, developmental-delay-(disorder), developmental-disabilities, epilepsy, impairment-(finding), language-development-disorders, language-disorders, learning-disabilities, malnutrition, muscle-hypotonia, pervasive-development-disorder, specific-language-impairment, speech-disorders.
Among the many pathways, these few ones have gauged particular interests from scientists studying Language Delays, and have been seen in publications frequently: Brain Development, Cell Adhesion, Cognition, Creatine Transport, Dishabituation, Embryo Development, Habituation, Localization, Mammary Gland Development, Meiosis, Myelination, Neurogenesis, Pathogenesis, Reflex, Segmentation, Social Behavior, Tooth Eruption, Translation, Transport
Quite a number of genes have been found to play important roles in Language Delays, such as ALDH5A1, CALB2, CD55, CNTNAP2, CR2, DHRS4, FMN1, FOXC2, FOXP2, GAMT, GTF2I, HES1, HMGCL, LIPC, NDP, NDUFB6, SEPHS1, SGCE, SLC6A8, TDGF1. 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.