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Results 1 - 10 of 29 for Corneal disorder
  1. Congenital stromal corneal dystrophy 
    ... Congenital Stromal Corneal Dystrophy National Organization for Rare Disorders (NORD) CORNEAL DYSTROPHY, CONGENITAL STROMAL; CSCD PubMed Bredrup C, Knappskog ...
    https://medlineplus.gov/.../congenital-stromal-corneal-dystrophy - Genetics
  2. Lattice corneal dystrophy type I 
    ... corneal dystrophy type I National Organization for Rare Disorders (NORD) CORNEAL DYSTROPHY, LATTICE TYPE I; CDL1 PubMed Kannabiran C, ...
    https://medlineplus.gov/.../lattice-corneal-dystrophy-type-i - Genetics
  3. Meesmann corneal dystrophy 
    ... also have temporary episodes of blurred vision. Meesmann corneal dystrophy is a rare disorder whose prevalence is unknown. It was first described ... dystrophy Meesmann corneal dystrophy National Organization for Rare Disorders (NORD) CORNEAL DYSTROPHY, MEESMANN, 1; MECD1 PubMed Corden LD, Swensson ...
    https://medlineplus.gov/.../condition/meesmann-corneal-dystrophy - Genetics
  4. APOE gene 
    ... pathogenesis of numerous clinical conditions including HSV-1 corneal disease. Exp Eye Res. 2007 May;84(5):801- ...
    https://medlineplus.gov/genetics/gene/apoe - Genetics
  5. Fuchs endothelial dystrophy 
    ... Registry: Corneal dystrophy, Fuchs endothelial, 1 Fuchs endothelial corneal dystrophy National Organization for Rare Disorders (NORD) ClinicalTrials.gov CORNEAL DYSTROPHY, FUCHS ENDOTHELIAL, 1; ...
    https://medlineplus.gov/.../condition/fuchs-endothelial-dystrophy - Genetics
  6. DCN gene 
    ... DCN gene have been associated with congenital stromal corneal dystrophy. This condition is an inherited eye disorder that causes the corneas to become cloudy. The ...
    https://medlineplus.gov/genetics/gene/dcn - Genetics
  7. Peters anomaly 
    ... This condition is one of a group of disorders known as congenital corneal opacities, which affect 3 to 6 individuals per ... as incomplete separation of eye structures and complete corneal opacity, or they can result in minor eye ... they occur in people with no apparent history of the disorder in their family. In many of these sporadic ...
    https://medlineplus.gov/genetics/condition/peters-anomaly - Genetics
  8. Fish-eye disease 
    ... and beta-LCAT activity lead to a related disorder called complete LCAT deficiency, which involves corneal opacities in combination with features affecting other parts ...
    https://medlineplus.gov/genetics/condition/fish-eye-disease - Genetics
  9. LCAT gene 
    ... identified in people with complete LCAT deficiency, a disorder that primarily causes corneal clouding and kidney problems. Individuals with complete LCAT ...
    https://medlineplus.gov/genetics/gene/lcat - Genetics
  10. Cystinosis 
    ... in affected individuals in adolescence. Malfunctioning kidneys and corneal crystals are the main initial features of this disorder. If intermediate cystinosis is left untreated, complete kidney ...
    https://medlineplus.gov/genetics/condition/cystinosis - Genetics
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