Drusen are discussed frequently in the context of their association with age-related macular
degeneration (AMD). Some types may, however, be regarded as a normal consequence of …

Background: Gene therapy cannot be yet considered a far perspective, but a tangible
therapeutic option in the field of retinal diseases. Although still confined in experimental …

Purpose: We evaluated the incongruous observation whereby flecks in recessive Stargardt
disease (STGD1) can exhibit increased short-wavelength autofluorescence (SW-AF) that …

Stargardt disease (STGD1) is an autosomal recessive retinal dystrophy, characterised by
bilateral progressive central vision loss and subretinal deposition of lipofuscin‐like …

Purpose.: To study the relationship between macular cone structure, fundus
autofluorescence (AF), and visual function in patients with Stargardt disease (STGD) …

Methods.: Thirty-three consecutive patients (48 eyes) underwent SD-OCT using the eye-
tracked follow-up protocol 24±2 months after baseline examination. Each pair of B-scans …

Purpose.: To measure macular visual function in patients with unstable fixation, to define the
photoreceptor source of this function, and to estimate its test-retest repeatability as a …

Since the discovery of the ABCA4 gene as the cause of autosomal recessive Stargardt
disease/fundus flavimaculatus much has been written of the phenotypic variability in ABCA4 …

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Importance The presence of choroidal hyperreflective foci in Stargardt disease is, to our
knowledge, a potentially new finding. Evaluation of these foci may aid in better …