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Stargardt disease
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Stargardt disease
Ricardo Leitão Guerra, MD59yo
Stargardt disease, associated with mutations in the ABCA4 gene, is the most common form of inherited juvenile macular degeneration. It is characterized by progressive loss of central vision,...
Stargardt disease, associated with mutations in the ABCA4 gene, is the most common form of inherited juvenile macular degeneration. It is characterized by progressive loss of central vision,...
Stargardt disease, associated with mutations in the ABCA4 gene, is the most common form of inherited juvenile macular degeneration. It is characterized by progressive loss of central vision, often beginning in childhood or adolescence. The disease leads to the accumulation of lipofuscin in the retinal pigment epithelium, visible as yellowish flecks on imaging studies, predominantly affecting the macula and central vision.
#retina #oftalmo #ophthalmology #oftalmologia #oftalmología #ophtalmologie #офтальмологія #офтальмология #οφθαλμολογία #retinography2024 #CIRRUS6000 #CLARUS700 #ZEISSRETINAWORKFLOW
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Stargardt disease
Ricardo Leitão Guerra, MD61yo
Stargardt disease, a genetic eye disorder, is characterized by central vision loss. Fundus autofluorescence (FAF) imaging is crucial for diagnosing and monitoring Stargardt disease by reveal...
Stargardt disease, a genetic eye disorder, is characterized by central vision loss. Fundus autofluorescence (FAF) imaging is crucial for diagnosing and monitoring Stargardt disease by reveal...
Stargardt disease, a genetic eye disorder, is characterized by central vision loss. Fundus autofluorescence (FAF) imaging is crucial for diagnosing and monitoring Stargardt disease by revealing characteristic flecks and areas of decreased autofluorescence due to lipofuscin accumulation in retinal pigment epithelial cells.
Disclosure: All images featured in this post were acquired and analyzed using devices integrated within the Zeiss Retina Workflow. This ensures high-quality, detailed visual data for comprehensive assessment.
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