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Fuchs dystrophy, also referred to as Fuchs endothelial corneal dystrophy (FECD) and Fuchs endothelial dystrophy (FED), is a slowly progressing corneal dystrophy that usually affects both eyes and is slightly more common in women than in men. Although early signs of Fuchs dystrophy are sometimes seen in people in their 30s and 40s, the disease ...
Codes following these are found at List of MeSH codes (C17). For other MeSH codes, ... MeSH C16.320.290.162.410 – Fuchs' endothelial dystrophy;
The following is a partial list of the "C" codes for Medical Subject Headings (MeSH), as defined by the United States National Library of Medicine (NLM). This list continues the information at List of MeSH codes (C10). Codes following these are found at List of MeSH codes (C12). For other MeSH codes, see List of MeSH codes.
This is a list of disorder codes in the Online Mendelian Inheritance in Man (OMIM) database. ... Corneal dystrophy, Fuchs endothelial, 4; 613268; SLC4A11;
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When affected by some reason, such as Fuchs' dystrophy or a trauma during cataract removal, endothelial cells suffer mortality or damage. [1] The corneal endothelial cells normally do not undergo mitotic cell division, and cell loss results in permanent loss of function.
Here are links to possibly useful sources of information about Fuchs' dystrophy. PubMed provides review articles from the past five years (limit to free review articles) The TRIP database provides clinical publications about evidence-based medicine. Other potential sources include: Centre for Reviews and Dissemination and CDC
Fleck corneal dystrophy, also known as Francois-Neetens speckled corneal dystrophy, is a rare form of corneal dystrophy. It is caused by mutations in PIKFYVE gene. Small opacities, some of which resemble "flecks", are scattered in the stroma of the patients. Other opacities look more like snowflakes or clouds.