Background: To investigate the prevalence of macular abnormalities in patients affected by Usher syndrome (USH), by comparing the clinical findings between two types (i.e., USH1 and USH2). Material and methods: A retrospective study was performed by reviewing optical coherence tomography (OCT) in 134 USH patients to determine the presence of macular abnormalities, including cystoid macular edema (CME), epiretinal membrane (ERM), vitreo-macular traction syndrome (VMT), and macular hole (MH). Results: Macular abnormalities were observed in 126/268 (47.0%) examined eyes. The most frequent abnormality was ERM observed in 51 eyes (19%), followed by CME observed in 42 eyes (15.7%). Moreover, CME was significantly (p < 0.05) associated with you...
Purpose: To determine optical coherence tomographic (OCT) features of macular edema (ME) and identif...
Background: This study aimed to compare phenotype–genotype correlation in patients with Usher syndro...
Objective: To characterize visual function in defined genotypes including siblings with Usher syndro...
Background: To investigate the prevalence of macular abnormalities in patients affected by Usher syn...
International audienceBackground: To evaluate novel grading system used to quantify optical coherenc...
Purpose: To investigate the functional and structural biomarkers and their correlation with Usher sy...
AbstractPurpose of this study was to characterize retinal disease in Usher syndrome using fundus aut...
International audiencePurpose: To describe retinal alterations detected by swept-source optical cohe...
Purpose: To calculate the prevalence of all vitreomacular interface (VMI) disorders and stratify acc...
PURPOSE: To calculate the prevalence of all vitreomacular interface (VMI) disorders and stratify acc...
AIM: To investigate the prevalence of macular abnormalities in a large Caucasian cohort of patients ...
Purpose : Natural history data of Usher Syndrome (USH) due to MYO7A mutations are scarce. In view of...
Purpose: The aim of this study is to report on the results of color vision testing in a European coh...
Background: This study aimed to compare phenotype-genotype correlation in patients with Usher syndro...
Background To investigate the risk of primary macular hole (MH) in the fellow eye, and to evaluate b...
Purpose: To determine optical coherence tomographic (OCT) features of macular edema (ME) and identif...
Background: This study aimed to compare phenotype–genotype correlation in patients with Usher syndro...
Objective: To characterize visual function in defined genotypes including siblings with Usher syndro...
Background: To investigate the prevalence of macular abnormalities in patients affected by Usher syn...
International audienceBackground: To evaluate novel grading system used to quantify optical coherenc...
Purpose: To investigate the functional and structural biomarkers and their correlation with Usher sy...
AbstractPurpose of this study was to characterize retinal disease in Usher syndrome using fundus aut...
International audiencePurpose: To describe retinal alterations detected by swept-source optical cohe...
Purpose: To calculate the prevalence of all vitreomacular interface (VMI) disorders and stratify acc...
PURPOSE: To calculate the prevalence of all vitreomacular interface (VMI) disorders and stratify acc...
AIM: To investigate the prevalence of macular abnormalities in a large Caucasian cohort of patients ...
Purpose : Natural history data of Usher Syndrome (USH) due to MYO7A mutations are scarce. In view of...
Purpose: The aim of this study is to report on the results of color vision testing in a European coh...
Background: This study aimed to compare phenotype-genotype correlation in patients with Usher syndro...
Background To investigate the risk of primary macular hole (MH) in the fellow eye, and to evaluate b...
Purpose: To determine optical coherence tomographic (OCT) features of macular edema (ME) and identif...
Background: This study aimed to compare phenotype–genotype correlation in patients with Usher syndro...
Objective: To characterize visual function in defined genotypes including siblings with Usher syndro...