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MeSH Review

Corneal Opacity

 
 
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Disease relevance of Corneal Opacity

 

Psychiatry related information on Corneal Opacity

 

High impact information on Corneal Opacity

 

Chemical compound and disease context of Corneal Opacity

 

Biological context of Corneal Opacity

 

Anatomical context of Corneal Opacity

 

Gene context of Corneal Opacity

  • Familial lecithin:cholesterol acyltransferase (LCAT) deficiency is a hereditary disorder with clinical manifestations including corneal opacity, premature atherosclerosis and renal failure [26].
  • Macular corneal dystrophy (MCD) is an autosomal recessive disease characterized by corneal opacities and caused by mutations in a carbohydrate sulfotransferase gene, known as CHST6 [27].
  • Cat4 is the second largest allelism group in the collection of mouse dominant eye mutations recovered in Neuherberg and carriers express anterior polar cataract, central corneal opacity, and lens-corneal adhesions [28].
  • Accumulating evidence suggests the involvement of TGF-beta in the process of corneal opacity, which is one of the serious causes of visual loss [29].
  • RESULTS: Corneal opacity in IL-6(-/-) mice was substantially diminished in comparison with IL-6(+/+) hosts 24 to 48 hours after intracorneal viral infection, and corneal levels of (MIP)-2 and MIP-1alpha were significantly reduced [30].
 

Analytical, diagnostic and therapeutic context of Corneal Opacity

References

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  19. Further genetic analysis of two autosomal dominant mouse eye defects, Ccw and Pax6(coop). Lyon, M.F., Bogani, D., Boyd, Y., Guillot, P., Favor, J. Mol. Vis. (2000) [Pubmed]
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  29. Blockade of TGF-beta by in vivo gene transfer of a soluble TGF-beta type II receptor in the muscle inhibits corneal opacification, edema and angiogenesis. Sakamoto, T., Ueno, H., Sonoda, K., Hisatomi, T., Shimizu, K., Ohashi, H., Inomata, H. Gene Ther. (2000) [Pubmed]
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