Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 10 of 16 for Corneal dystrophy
  1. Meesmann corneal dystrophy is an eye disease that affects the cornea, which is the clear front covering of the eye. This condition is characterized by the formation ...
  2. Lattice corneal dystrophy type II is characterized by an accumulation of protein clumps called amyloid deposits in tissues throughout the ... accumulation of amyloid deposits in the cornea (lattice corneal dystrophy). The cornea is the clear, outer covering of ...
  3. Congenital stromal corneal dystrophy is an inherited eye disorder. This condition primarily affects the cornea, which is the clear outer covering of the eye. In ...
  4. Lattice corneal dystrophy type I is an eye disorder that affects the clear, outer covering of the eye called the ... an individual to see properly; however, in lattice corneal dystrophy type I, protein clumps known as amyloid deposits ...
  5. ... the disorder in their family. Fuchs atrophy Fuchs corneal dystrophy Fuchs dystrophy Fuchs endothelial corneal dystrophy Fuchs' endothelial dystrophy Genetic Testing Registry: Corneal dystrophy, ...
  6. ... Bietti crystalline retinopathy Bietti tapetoretinal degeneration with marginal corneal dystrophy Genetic Testing Registry: Bietti crystalline corneoretinal dystrophy Bietti ...
  7. ... LCAT deficiency Alpha-lecithin:cholesterol acyltransferase deficiency Dyslipoproteinemic corneal dystrophy FED LCATA deficiency Partial LCAT deficiency Genetic Testing ...
  8. Tyrosinemia is a genetic disorder characterized by problems breaking down the amino acid tyrosine, which is a building block of most proteins. If the condition is ...
  9. ... mutations in the TGFBI gene can cause lattice corneal dystrophy type I. This inherited eye condition is characterized ... up of several layers of tissue. In lattice corneal dystrophy type I, the deposits occur in the stromal ...
  10. ... KRT3 gene have been found to cause Meesmann corneal dystrophy, an eye disease characterized by the formation of ... the identified KRT3 gene mutations associated with Meesmann corneal dystrophy change single protein building blocks (amino acids) in ...
previous · 1 · 2 · next