Publications by authors named "Ester Carreno Salas"
Article Synopsis
- The study aimed to explore the relationship between genetic variants and visual outcomes in patients with retinopathy.
- Three patient groups were analyzed based on genetic variants: two loss-of-function (TLOF), two missense (TM), and one of each (MLOF).
- Results showed that patients with missense variants (TM) had better visual acuity and structural integrity compared to those with TLOF, suggesting differences in prognosis and implications for future gene therapy.
Introduction: Biallelic pathogenic RPE65 variants are related to a spectrum of clinically overlapping inherited retinal dystrophies (IRD). Most affected individuals progress to severe disease, with 50% of patients becoming legally blind by 20 years of age. Deeper knowledge of the mutational spectrum and the phenotype-genotype correlation in RPE65-related IRD is needed.
View Article and Find Full Text PDFAim: To standardise the nomenclature for reporting optical coherence angiography (OCT-A) findings in the field of uveitis.
Methods: Members of the International Uveitis Study Group, of the American Uveitis Society and of the Sociedad Panamericana de Infermedades Oculares that choose to participate responded to an online questionnaire about their preferred terminology when reporting on OCT-A findings in uveitis. The response of individuals with several publications on OCT-A (experts) was compared with uveitis specialists (users) who have less than five publications on the field of uveitis and OCT-A.
Introduction: To report the spectrum and frequency of conjunctiva tumours in an ocular oncology unit analysing the clinical profile of benign, precancerous and malignant conjunctival lesions.
Methods: A retrospective case series of 462 consecutive patients diagnosed at the Ocular Oncology Unit of the University Hospital of Valladolid from 1992 to 2017.
Results: Among 462 consecutive patients, the tumour was classified as melanocytic in 252 (54.