Aicardi's Syndrome

Overview of Aicardi's Syndrome

Most recent studies have shown that Aicardi's Syndrome shares some biological mechanisms with agenesis-of-corpus-callosum, brain-diseases, chorioretinal-disorder, choroid-diseases, congenital-abnormality, congenital-absence, congenital-ocular-coloboma-(disorder), developmental-delay-(disorder), developmental-disabilities, epilepsy, eye-abnormalities, hypoplasia, infantile-spasms, microphthalmos, neoplasms, polymicrogyria, retinal-diseases, spasm.

Among the many pathways, these few ones have gauged particular interests from scientists studying Aicardi's Syndrome, and have been seen in publications frequently: Brain Development, Chromosome Breakage, Dosage Compensation, Localization, Methylation, Muscle Contraction, Myelination, Oogenesis, Pathogenesis, Pigmentation, Reflex, Segmentation

Quite a number of genes have been found to play important roles in Aicardi's Syndrome, such as AR, BCL9, CDKL5, CHP1, DCTN3, DYNC1H1, EXT1, FBN2, FLNA, GPM6A, GPM6B, IKBKG, MECP2, MSL3, PHB2, POMC. 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.

Aicardi's Syndrome Related Genes

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Pathways Related to Aicardi's Syndrome

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

Related Diseases