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7 Cards in this Set
- Front
- Back
- 3rd side (hint)
Sign? Dx? |
Vogt striae Keratoconus |
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37 yo w progressive decline of va and glare. Va 20/100 ou. PE: brow ptosis ou Dx? Hint: question 2 |
lattice corneal dystrophy type II (LCD2), familial amyloid polyneuropathy type 4, meretoja syndrome is a systemic amyloidosis with severe manifestations in the skin, cranial nerves and cornea. It is AD and usually presents on the third decade of life. Q2. Salzmann nodules
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Q2. Name of sign on inferior cornea? |
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30yo w increasing haze. 50y Father has completely hazed cornea |
Schnyder Corneal Dystrophy AD mut in ubiad1 gene. Onset 20-30s Completely hazed cornea by 50y Cholesterol and phospholipid deposition, arcus senilis |
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Hint for Hx |
Fuchs endothelial dystrophy - blurry vision morning (fluid accumulation, eyes closed) -ruptured blisters/cyst=pain -F>M. -Sxs usually start when 50+ |
50y F blurry vision in the mornings |
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Front (Term) |
Fuchs endothelial dystrophy, AD dystrophy, presents w/ decreased Va worse AM. Mild=guttate, severe=bullae, scarring and bullous keratopathy |
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Sign? Dx? |
Haab Striae Seen in 1ry cong. Glaucoma -breaks in Descemet (horizontal/concentric & curvilinear) - ddx of PPMD
- horizontal |
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Front (Term) |
Peripheral Ulcerative Keratitis PUK Inflammatory peripheral corneal thinning Causes: RA, collagen vasc diseases, ibd. Vasculitides (pan, wegener) Moorens ulcer: usually includes limbus (other puk causes spare it) Rheumatoid furrow Ddx: peripheral corneal DEGENERATIONS-!terriens marginal deg, pellucid marginal deg, Senile Furrow Deg |
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