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Disease Info Card
Meige Syndrome
Information about Meige 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 Meige Syndrome
Most recent studies have shown that Meige Syndrome shares some biological mechanisms with basal-ganglia-diseases, blepharoptosis, blepharospasm, dyskinetic-syndrome, dystonia-disorders, dystonia-musculorum-deformans, eyelid-diseases, focal-dystonia, generalized-dystonia, involuntary-movements, lingual-facial-buccal-dyskinesia, movement-disorders, muscle-cramp, parkinson-disease, spasm, spasmodic-dysphonia, torticollis.
Among the many pathways, these few ones have gauged particular interests from scientists studying Meige Syndrome, and have been seen in publications frequently: Blood Circulation, Dedifferentiation, Excretion, Hypersensitivity, Innervation, Localization, Mastication, Muscle Atrophy, Muscle Contraction, Pathogenesis, Proprioception, Reflex, Regeneration, Secretion, Sensory Processing, Transport
Quite a number of genes have been found to play important roles in Meige Syndrome, such as ARNTL, ARSA, BLM, CAMP, CD1B, CD1E, CD82, CDCA7L, GNPDA1, GP1BB, GPI, LRP2, MAMLD1, MCF2L, OMD, RRM1, RRM2, THAP1, TOR1A. 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.