17 corneal dystrophies
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Transcript of 17 corneal dystrophies
![Page 1: 17 corneal dystrophies](https://reader036.fdocuments.in/reader036/viewer/2022062523/58efaf7b1a28ab31278b46af/html5/thumbnails/1.jpg)
CORNEAL DYSTROPHIES1. Anterior• Cogan microcystic• Reis-Bucklers• Meesmann• Schnyder
2. Stromal• Lattice I, II, III• Granular I, II, III (Avellino)• Macular
3. Posterior• Fuchs endothelial• Posterior polymorphous
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Cogan microcystic dystrophy• Most common of all dystrophies• Neither familial nor progressive• Recurrent corneal erosions in about 10% of cases
Dots
Fingerprints
Cysts
Maps
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Four types of lesions - in isolation or combinationMicrocystsDots
Maps Fingerprints
Signs of Cogan dystrophy
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Inheritance - autosomal dominantOnset - early childhood with recurrent corneal erosions
Superficial polygonal opacities
Honeycomb appearance
Treatment - keratoplasty if severe
Reis-Bucklers dystrophy..
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Meesmann dystrophyInheritance - autosomal dominantOnset - first decade with mild visual symptoms
Treatment - not required
• Clear in retroillumination• Grey in direct illumination
• Tiny, epithelial cysts, maximal centrally
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Inheritance - autosomal dominantOnset - second decade with visual impairment
Treatment - excimer laser keratectomy
Schnyder dystrophy
Subepithelial ‘crystalline’ opacities
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Inheritance - autosomal dominantOnset - late first decade with recurrent corneal erosions
Treatment - penetrating keratoplasty if severe
Lattice dystrophy type I
Fine, spidery, branching lines within stroma
Later general haze may submerge lesions
Progression
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Inheritance Autosomal dominant
Onset Middle age with progressive facial palsy and lattice dystrophy identical to type I
Systemic features• Cranial and peripheral neuropathy• Skin laxity• Renal and cardiac failure
Treatment Penetrating keratoplasty if severe
Lattice dystrophy type II(Familial amyloidosis with lattice dystrophy, Meretoja syndrome)
Mask-like facies
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Inheritance - autosomal dominantOnset - fourth decade
• Thick, ropey lines and minimal intervening haze• May be asymmetrical and initially unilateral
Treatment - penetrating keratoplasty if severe
Lattice dystrophy type III
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Inheritance - autosomal dominantOnset - first decade with recurrent corneal erosions
Treatment - penetrating keratoplasty if severe
Granular dystrophy type I
Eventual confluenceInitial superficial andcentral crumb-like opacities
Later deeper and peripheral spread but limbus spared
Progression
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Inheritance - autosomal dominantOnset - fourth or fifth decade with mild recurrent erosions
Superficial, discrete crumb-like opacitiesTreatment - penetrating keratoplasty if severe
Granular dystrophy type II
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Inheritance - autosomal dominantOnset - late in life; frequently asymptomatic
• Few, superficial, discrete, ring-shaped lesions• Increase in density and size with time
Treatment - not required
Granular dystrophy type III (Avellino)
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Inheritance - autosomal recessiveOnset - second decade with painless visual loss
Macular dystrophy
Treatment - penetrating keratoplasty
Initial dense, poorly delineated opacities
Later generalized opacification
Thinning
Progression
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Inheritance - occasionally autosomal dominantOnset - old age
Treatment - penetrating keratoplasty if advanced
Fuchs endothelial dystrophy
Eventually bullous keratopathy
Later central stromal oedema
Gradual increase in cornea guttata with peripheral spread
Progression
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Inheritance - usually autosomal dominantOnset - difficult to determine because asymptomatic
• Subtle, vesicular, geographic, or band-like lesions• Frequently asymmetrical
Treatment - not required
Posterior polymorphous dystrophy