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Disease Info Card
Macular Corneal Dystrophy
Information about Macular Corneal Dystrophy: 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 Macular Corneal Dystrophy
Most recent studies have shown that Macular Corneal Dystrophy shares some biological mechanisms with age-related-macular-degeneration, amyloidosis, blind-vision, corneal-diseases, dystrophy, familial-amyloid-polyneuropathy-type-v, fuchs-endothelial-dystrophy, granular-corneal-dystrophy, hereditary-corneal-dystrophy, hereditary-diseases, keratitis, macular-corneal-dystrophy-type-i, mucopolysaccharidoses, mucopolysaccharidosis-i, storage-disease, stromal-corneal-dystrophy, visual-impairment.
Among the many pathways, these few ones have gauged particular interests from scientists studying Macular Corneal Dystrophy, and have been seen in publications frequently: Dehiscence, Delamination, Glycosylation, Localization, Pathogenesis, Secretion, Sulfation, Wound Healing
Quite a number of genes have been found to play important roles in Macular Corneal Dystrophy, such as A4GALT, ABCB6, CHST6, COL18A1, DMPK, EGF, GALNS, GLB1, GSN, LUM, MLYCD, OGN, OXSM, STS, TGFBI. 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.
Pathways Related to Macular Corneal Dystrophy
This information is being compiled and will come in a future update
| Dehiscence | Delamination | Glycosylation |
| Localization | Pathogenesis | Secretion |
| Sulfation | Wound Healing |