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  2. Fuchs' dystrophy - Wikipedia

    en.wikipedia.org/wiki/Fuchs'_dystrophy

    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 ...

  3. Talk:Fuchs' dystrophy - Wikipedia

    en.wikipedia.org/wiki/Talk:Fuchs'_dystrophy

    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

  4. Fuchs's dystrophy - Wikipedia

    en.wikipedia.org/?title=Fuchs's_dystrophy...

    From Wikipedia, the free encyclopedia. Redirect page

  5. Descemet's membrane - Wikipedia

    en.wikipedia.org/wiki/Descemet's_membrane

    Copper disposition on corneal Descemet's membrane. Significant damage to the membrane may require a corneal transplant. Damage caused by the hereditary condition known as Fuchs dystrophy (q.v.)—where Descemet's membrane progressively fails and the cornea thickens and clouds because the exchange of nutrients/fluids between the cornea and the rest of the eye is interrupted—can be reversed by ...

  6. List of OMIM disorder codes - Wikipedia

    en.wikipedia.org/wiki/List_of_OMIM_disorder_codes

    This is a list of disorder codes in the Online Mendelian Inheritance in Man (OMIM) database. These are diseases that can be inherited via a Mendelian genetic mechanism. OMIM is one of the databases housed in the U.S. National Center for Biotechnology Information.

  7. Bullous keratopathy - Wikipedia

    en.wikipedia.org/wiki/Bullous_keratopathy

    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.

  8. Category:Diseases named after discoverers - Wikipedia

    en.wikipedia.org/wiki/Category:Diseases_named...

    A. Aarskog–Scott syndrome; Aase syndrome; Abdallat–Davis–Farrage syndrome; Abruzzo–Erickson syndrome; Achard–Thiers syndrome; Adams–Nance syndrome

  9. Fleck corneal dystrophy - Wikipedia

    en.wikipedia.org/wiki/Fleck_corneal_dystrophy

    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.