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Journals / Retina-Vitreus / 2020 / Cilt: 29 - Sayı: 2

Central Areolar Choroidal Dystrophy Case

Cafer TANRIVERDİ
Burcu NURÖZLER TABAKCI
Fevzi ŞENTÜRK
Pages
152–156
DOI
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

Here, we aimed to review clinicalfi ndings, ophthalmological imaging results and electrodiagnostic test results in a 43-years old man presented with visual impairment to ourclinic and diagnosed as central areolar choroidal dystrophy.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Central areolar choroidal dystrophy is a rarely seen, hereditary retinal disease which primarily affects macula.
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Key Findings & Data:Central areolar choroidal dystrophy is a rarely seen, hereditary retinal disease which primarily affects macula.
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Conclusion & Impact:Here, we aimed to review clinicalfi ndings, ophthalmological imaging results and electrodiagnostic test results in a 43-years old man presented with visual impairment to ourclinic and diagnosed as central areolar choroidal dystrophy.
🔬Design:Review & Systematic Survey
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Özet

Central areolar choroidal dystrophy is a rarely seen, hereditary retinal disease which primarily affects macula. Here, we aimed to review clinicalfi ndings, ophthalmological imaging results and electrodiagnostic test results in a 43-years old man presented with visual impairment to ourclinic and diagnosed as central areolar choroidal dystrophy.

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Cite This Article

TANRIVERDİ, C., TABAKCI, B. N., ŞENTÜRK, F. (2020). Central Areolar Choroidal Dystrophy Case. Retina-Vitreus, Cilt: 29 - Sayı: 2, 152–156. https://ajindex.com/articles/340341

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