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Rod sensitivity is compromised in many retinal pathologies like pigmentary retinopathy, rod-cone dystrophy, retinal telangiectasia, congenital night blindness, and central serous chorioretinitis.
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This is of special interest as many retinal degenerative diseases are not developmental pathologies.
Evaluation of spatial agreement between UWF FAF and GVF has been performed in other retinal pathologies, such as retinitis pigmentosa [13].
Disruption of RPE phagocytosis is causal to severe retinal pathologies, such as retinitis pigmentosa and rod/cone dystrophies.
Malfunctions of these processes or other pathological reactions often precipitate severe retinal pathologies.
There are many possible solutions for modification of our algorithm to handle these retinal pathologies.
Functional OCT promises to enable the differentiation of retinal pathologies via localized, functional retinal response or metabolic properties.
With the increased prevalence of retinal pathologies, automating the detection of these pathologies is becoming more and more relevant.
No treatments exist to effectively treat many retinal diseases.
Marfan syndrome patients often have retinal pathologies.
Three patients were excluded from OCT analysis due to non-MS related retinal pathologies.
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