Prospective Cohort Study of Childhood-Onset Stargardt Disease: Fundus Autofluorescence Imaging, Progression, Comparison with Adult-Onset Disease, and Disease Symmetry

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Progression of Late-Onset Stargardt Disease.

Purpose Identification of sensitive biomarkers is essential to determine potential effects of emerging therapeutic trials for Stargardt disease. This study aimed to describe the natural history of late-onset Stargardt, and demonstrates the accuracy of retinal pigment epithelium (RPE) atrophy progression as an outcome measure. Methods We performed a retrospective cohort study collecting multic...

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Quantitative fundus autofluorescence in recessive Stargardt disease.

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Fine central macular dots associated with childhood-onset Stargardt Disease.

Booij JC, Baas DC, Beisekeeva J, Gorgels TG & Bergen AA (2010): The dynamic nature of Bruch’s membrane. Prog Retin Eye Res 29: 1–18. Finger RP, Charbel Issa P, Schmitz-Valckenberg S, Holz FG & Scholl HN (2011): Longterm effectiveness of intravitreal bevacizumab for choroidal neovascularization secondary to angioid streaks in pseudoxanthoma elasticum. Retina 31: 1268–1278. Gliem M, De Zeaytijd J...

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Clinical and Molecular Characteristics of Childhood-Onset Stargardt Disease

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Fundus autofluorescence patterns in stargardt disease over time.

OBJECTIVE To study the longitudinal changes in autofluorescence in Stargardt disease to reveal aspects of disease progression not previously evident. Changes in autofluorescence reflect changing fluorophore compositions of lipofuscin and melanin in retinal pigment epithelial cells, which has been hypothesized to contribute to Stargardt disease pathogenesis. METHODS We examined the temporospat...

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ژورنال

عنوان ژورنال: American Journal of Ophthalmology

سال: 2020

ISSN: 0002-9394

DOI: 10.1016/j.ajo.2019.11.008