Results 1 to 10 of about 59 (59)
Cellular and Molecular Mechanisms of Pathogenesis Underlying Inherited Retinal Dystrophies
Biomolecules, 2023 Inherited retinal dystrophies (IRDs) are congenital retinal degenerative diseases that have various inheritance patterns, including dominant, recessive, X-linked, and mitochondrial.
Andrew Manley +3 more
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Oftalʹmologiâ, 2021 Aim: to study genotype-phenotype correlations in patients with inherited retinal diseases with mutations in ABCA4 gene in Russian Federation.Patients and methods.
I. V. Zolnikova +9 more
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Multimodal Imaging in a Case of Stargardt’s Disease
Delhi Journal of Ophthalmology, 2022 Stargardt Disease is the most common macular dystrophy, and multimodal image can be used for diagnosis and monitoring of the disease.
Shruti Bhattacharya +3 more
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Depression and quality of life in individuals with Stargardt’s disease [PDF]
Jornal Brasileiro de Psiquiatria, 2020 Objectives To assess depression and quality of life in individuals with Stargardt’s disease (SD), macular dystrophy whose central vision loss begins in the first decades of life.
Mirela L. S. Gomes +5 more
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Kinetics of Heterogeneous Background in Stargardt’s Disease over Time
Life, 2022 Stargardt’s disease (STGD1) is caused by mutations in the ABCA4 gene. Different lesions characterised by decreased autofluorescence levels are found in fundus autofluorescence (FAF) from STGD1 patients and could be used as outcome indicators for disease ...
Eduardo Rodríguez-Bocanegra +5 more
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Vitamin A, systemic T-cells, and the eye: Focus on degenerative retinal disease
Frontiers in Nutrition, 2022 The first discovered vitamin, vitamin A, exists in a range of forms, primarily retinoids and provitamin carotenoids. The bioactive forms of vitamin A, retinol and retinoic acid, have many critical functions in body systems including the eye and immune ...
Arun J. Thirunavukarasu +4 more
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Inherited Macular Dystrophies in a Tertiary Care Centre
Journal of Nepal Health Research Council, 2020 Background: Inherited macular dystrophies constitute a group of diseases characterized by bilateral central visual loss with symmetrical macular abnormalities usually presenting in the first two decades of life.
Priyanka Shrestha +7 more
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Journal of Optometry, 2011 Purpose: To evaluate the ability of the preferential hyperacuity perimeter (PHP) and the Amsler grid to detect central scotomas in Stargardt's disease and age macular degeneration.
Eva Chamorro +2 more
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Management Of Stargardt’s Disease Through Ayurvedic Science
Delhi Journal of Ophthalmology, 2018 Stargardt’s disease is a hereditary disorder of the retina. There is a gradual loss of vision during childhood or adolescence and in a few cases, vision loss may be noticed in adulthood.
Santosh Kumar Shaw +2 more
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Journal of the Formosan Medical Association, 2013 Stargardt’s disease is the most common form of juvenile macular dystrophy. The purpose of this study is to report the clinical characteristics, visual function, and retinal tomography of patients diagnosed with Stargardt’s disease in Taiwan.
Jen-Pin Sun +5 more
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