The development of ultra-widefield retinal imaging has accelerated our understanding of
common retinal diseases. As we continue to validate the diagnostic and prognostic …

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

Purpose To explore fundus autofluorescence (FAF) imaging as an alternative to
electroretinography as a noninvasive, quick, and readily interpretable method to predict …

Stargardt macular degeneration (STGD) is a central blinding disease caused by loss of or
dysfunctional ABCA4 transporter in both photoreceptors and retinal pigment epithelial (RPE) …

Background Inherited retinal degeneration (IRD) refers to a heterogenous group of
progressive diseases that cause death of photoreceptor cells and subsequent vision loss …

Purpose Pathogenic variations in the ABCA4 gene are a leading cause of vision loss in
patients with inherited retinal diseases. ABCA4–retinal dystrophies are clinically …

Inherited retinal dystrophies (IRD) are a heterogeneous group of rare chronic disorders
caused by genetically determined degeneration of photoreceptors and retinal pigment …

The aim of this review article is to describe the specific features of Stargardt disease and
ABCA4 retinopathies (ABCA4R) using multimodal imaging and functional testing and to …

Purpose: To establish a mutation-specific age-dependent ultra-widefield fundus
autofluorescence (UWF-FAF) trajectory in a large Stargardt disease (STGD1) cohort using …

Inherited retinal diseases (IRDs) represent one of the major causes of progressive and
irreversible vision loss in the working-age population. Over the last few decades, advances …