Purpose: The purpose of this study was to present our findings on the natural history of late-onset retinal degeneration (LORD) in patients with molecularly confirmed C1QTNF5 heterozygous pathogenic variants and assess suitability of retinal structure parameters for disease monitoring. Methods: Sixteen patients with C1QTNF5-LORD were retrospectively identified from Moorfields Eye Hospital, UK. Fundus autofluorescence (FAF), optical coherence tomography (OCT) scans, and best-corrected visual acuity (BCVA) were collected. Area of atrophy (AA) was manually drawn in FAF images. Ellipsoid zone (EZ) width and foveal retinal thickness of the whole retina and outer retina were extracted from OCT scans. Agerelated changes were tested with linear-mix...
PURPOSE: To study the disease course of RPE65-associated inherited retinal degenerations (IRDs) as a...
ObjectiveWhile Alzheimer’s disease is associated with inner retina thinning measured by spectral-dom...
Purpose: To investigate the natural history of RHO-associated retinitis pigmentosa (RP). Methods: A ...
PurposeTo characterize longitudinal structural changes in early stages of late-onset retinal degener...
Purpose: To investigate the natural history in patients with LRAT-associated retinal degenerations (...
Background: Late-onset retinal degeneration (L-ORD) is a rare autosomal dominant retinal dystrophy r...
Purpose: To describe the phenotypic spectrum of retinal disease caused by the c.2991+1655A>G mutatio...
Purpose: To study the disease course ofRPE65-associated inherited retinal degenerations (IRDs) as a ...
Aim: To describe the clinical and molecular features of a novel, autosomal dominant RDH12-retinopath...
PURPOSE: To describe the clinical, spectral-domain optical coherence tomography and electrophysiolog...
PURPOSE: To review and describe in detail the clinical course, functional and anatomical characteris...
Objectives: Bietti Crystalline Dystrophy (BCD) is an autosomal recessive progressive retinal diseas...
PURPOSE: To longitudinally characterize structural retinal changes in achromatopsia (ACHM) over ext...
BACKGROUND: Defects in retinol dehydrogenase 12 (RDH12) account for 3.4%-10.5 % of Leber congenital ...
PURPOSE: To determine the genetic background of sector retinitis pigmentosa (RP), natural history, i...
PURPOSE: To study the disease course of RPE65-associated inherited retinal degenerations (IRDs) as a...
ObjectiveWhile Alzheimer’s disease is associated with inner retina thinning measured by spectral-dom...
Purpose: To investigate the natural history of RHO-associated retinitis pigmentosa (RP). Methods: A ...
PurposeTo characterize longitudinal structural changes in early stages of late-onset retinal degener...
Purpose: To investigate the natural history in patients with LRAT-associated retinal degenerations (...
Background: Late-onset retinal degeneration (L-ORD) is a rare autosomal dominant retinal dystrophy r...
Purpose: To describe the phenotypic spectrum of retinal disease caused by the c.2991+1655A>G mutatio...
Purpose: To study the disease course ofRPE65-associated inherited retinal degenerations (IRDs) as a ...
Aim: To describe the clinical and molecular features of a novel, autosomal dominant RDH12-retinopath...
PURPOSE: To describe the clinical, spectral-domain optical coherence tomography and electrophysiolog...
PURPOSE: To review and describe in detail the clinical course, functional and anatomical characteris...
Objectives: Bietti Crystalline Dystrophy (BCD) is an autosomal recessive progressive retinal diseas...
PURPOSE: To longitudinally characterize structural retinal changes in achromatopsia (ACHM) over ext...
BACKGROUND: Defects in retinol dehydrogenase 12 (RDH12) account for 3.4%-10.5 % of Leber congenital ...
PURPOSE: To determine the genetic background of sector retinitis pigmentosa (RP), natural history, i...
PURPOSE: To study the disease course of RPE65-associated inherited retinal degenerations (IRDs) as a...
ObjectiveWhile Alzheimer’s disease is associated with inner retina thinning measured by spectral-dom...
Purpose: To investigate the natural history of RHO-associated retinitis pigmentosa (RP). Methods: A ...