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Disease Info Card
Acrocallosal Syndrome
Information about Acrocallosal Syndrome: 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 Acrocallosal Syndrome
Most recent studies have shown that Acrocallosal Syndrome shares some biological mechanisms with agenesis-of-corpus-callosum, congenital-abnormality, congenital-absence, congenital-hand-deformities, congenital-partial-absence, craniofacial-abnormalities, developmental-delay-(disorder), epilepsy, greig-cephalopolysyndactyly-syndrome, hydrocephalus, hypoplasia, macrocephaly, muscle-hypotonia, orbital-separation-excessive, polydactyly, polysyndactyly, severe-mental-retardation, syndactyly.
Among the many pathways, these few ones have gauged particular interests from scientists studying Acrocallosal Syndrome, and have been seen in publications frequently: Amelogenesis, Autolysis, Brain Development, Cell Adhesion, Cell Growth, Central Nervous System Development, Cognition, Corpus Callosum Development, Dna Methylation, Localization, Methylation, Myelination, Nervous System Development, Pathogenesis, Regeneration, System Development, Tooth Eruption
Quite a number of genes have been found to play important roles in Acrocallosal Syndrome, such as ABCA4, ACACA, ATAT1, ATP6V0A1, CCM2, FBN2, GLI3, IHH, KIF7, L1CAM, MED12, RFC1, RFC2, RFC4, SATB2, SHH, VCAM1. 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.