MeSH tree: E01.370.405.270
Congenital stationary night blindness (CSNB) is caused by mutations in a specific calcium channel. A comprehensive proteomic study by researchers at the University of Innsbruck now reveals how these mutations trigger complex, ...
Feb 2, 2026
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Texture analysis can identify retinal changes during early stages of type 2 diabetes, according to a study published in Eye Vision.
Dec 16, 2025
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Retinitis pigmentosa retinal degeneration is caused by a family of hereditary mutations in nearly 100 genes that slowly lead to blindness over years or decades.
Aug 29, 2025
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Electroretinography (ERG) is an ophthalmic diagnostic method used to determine whether the retina is functioning normally. It is widely employed for diagnosing hereditary retinal diseases or assessing retinal function decline.
Aug 12, 2025
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A multicenter study led by researchers from the State Key Laboratory of Ophthalmology in China has characterized a distinct retinal disorder in children following high fever illness. The study describes hyperacute outer retinal ...
Photoreceptors are the fundamental component of the entire vision process. These specialized cells that absorb light and trigger a specific physiological reaction in the body come in two varieties: cones (responsible for ...
Jun 6, 2024
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Eye diseases are becoming more prevalent worldwide, partly because of the aging population, but also because of our greatly increased screen time compared to previous generations. Considering the use of displays will most ...
May 13, 2024
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With a single flash of light to the eye, artificial intelligence (AI) could deliver a faster and more accurate way to diagnose autism spectrum disorder (ASD) in children, according to a new study from the University of South ...
Dec 18, 2023
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Retinal degeneration in the disease retinitis pigmentosa is caused by a family of hereditary mutations that slowly lead to blindness over years or decades. A mouse model of one of these forms of retinitis pigmentosa, RP59, ...
Oct 31, 2023
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