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cornea dystrophy

Corneal Dystrophies
Group of progressive , usually bilateral , mostly
genetically determined , non inflammatory opacifying
disorders

Classification

Epithelial

Bowman layer

Stromal

Endothelial
Epithelial dystrophies

Cogan epithelial basement membrane


dystrophy

Meesman epithelial dystrophy

Lisch epithelial dystrophy


Epithelial dystrophies

Sporadic

Histology

Thick basement membrane

Deposits of fibrillary protein

Absence of hemidesmosomes
Epithelial dystrophies
Onset

Signs

Dot like opacities

Epithelial microcyst

Subepithelial map like pattern

Whorled fingerprint – like lines


Lisch epithelial dystrophy
Inheritance

AD or XLD

Gene locus on Xp 22.3 in XLD

Signs

Grey band with whorls

Densely packed microcysts


Reis – Bucklers
dystrophy
Signs:

Grey white , fine ,round and polygonal

subepithelial opacities

Treatment:

Directed at recurrent errosions

Excimer laser keratectomy


Endothelial
dystrophies
Signs

Corneal guttata

Beaten metal appearance

Stromal edema

Epithelial edema

Microcyst and bullae


Symptoms of Corneal Dystrophies

• Watery eyes
• Dry eyes
• Glare
• Sensitivity to light
• Pain in the eye
• The feel of something in your eye
• Corneal erosions
Pathophysiology
A corneal dystrophy can be caused by an
accumulation of extraneous material in the
cornea, including lipids and cholesterol crystals.
Mooren’s Ulcer

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