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Results 1 - 7 of 7 for Lattice corneal dystrophy Type I
  1. Lattice corneal dystrophy type II is characterized by an accumulation of protein clumps called amyloid deposits in tissues throughout the body. The deposits ...
  2. ... is still a rare condition. The prevalence of lattice corneal dystrophy type I is unknown. Lattice corneal dystrophy type I ... Xie LX. An R124C mutation in TGFBI caused lattice corneal dystrophy type I with a variable phenotype in three Chinese ...
  3. ... dystrophy, including Groenouw corneal dystrophy, Avellino corneal dystrophy, lattice corneal dystrophy type IIIA, Reis-Bucklers corneal dystrophy, Thiel-Behnke corneal ...
  4. ... least two mutations in the GSN gene cause lattice corneal dystrophy type II. This condition is characterized by the accumulation ... the gelsolin protein.GSN gene mutations that cause lattice corneal dystrophy type II change a single protein building block (amino ...
  5. Corneal Disorders (National Library of Medicine)  
    Your cornea is the outermost layer of your eye. It is clear and shaped like a dome. The cornea helps to shield the rest of the eye from germs, dust, and other ...
  6. Amyloidosis (National Library of Medicine)  
    Amyloidosis occurs when abnormal proteins called amyloids build up and form deposits. The deposits can collect in organs such as the kidney and heart. This can cause ...
  7. Eye Diseases (National Library of Medicine)  
    Some eye problems are minor and don't last long. But some can lead to a permanent loss of vision. Common eye problems include: Refractive errors Cataracts - ...