Optometry and vision science : official publication of the American Academy of Optometry · 2026
Case series: The value of fundus autofluorescence in inherited macular disease.
СтатьяКлинический случайНазвание и аннотация: Перевод в очереди
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Guro Marina, Wang Henrietta, Phu Jack, Patel Nimesh B, Sapoznik Kaitlyn A, Shah Hamza, Kalloniatis Michael
Аннотация
PURPOSE: To evaluate the diagnostic utility of fundus autofluorescence (FAF) imaging in identifying and characterizing phenotypically classified inherited macular dystrophies. In this way, we aim to provide methods by which eye care practitioners can link FAF imaging and other clinical results or imaging modalities to aid their clinical decision-making.
CASE REPORTS: Phenotypically identified inherited macular dystrophies, including Stargardt disease and related ABCA4 mutations, Best vitelliform dystrophy, pattern dystrophies, and cone and cone-rod dystrophies, are discussed.
CONCLUSIONS: We provide evidence that the use of FAF alone and in combination with other clinical results and imaging modalities can assist in the diagnosis of a range of inherited macular dystrophies.
CASE REPORTS: Phenotypically identified inherited macular dystrophies, including Stargardt disease and related ABCA4 mutations, Best vitelliform dystrophy, pattern dystrophies, and cone and cone-rod dystrophies, are discussed.
CONCLUSIONS: We provide evidence that the use of FAF alone and in combination with other clinical results and imaging modalities can assist in the diagnosis of a range of inherited macular dystrophies.