دورية أكاديمية

Exploring self-reported visual function and vision-related anxiety in patients with RPGR-associated retinal degeneration

التفاصيل البيبلوغرافية
العنوان: Exploring self-reported visual function and vision-related anxiety in patients with RPGR-associated retinal degeneration
المؤلفون: Nuno Gouveia, Oluji Chukwunalu, Carolina Oliveira, C. Henrique Alves, Rufino Silva, Joaquim Murta, João Pedro Marques
المصدر: Scientific Reports, Vol 14, Iss 1, Pp 1-8 (2024)
بيانات النشر: Nature Portfolio, 2024.
سنة النشر: 2024
المجموعة: LCC:Medicine
LCC:Science
مصطلحات موضوعية: Patient-reported outcomes, Retinitis pigmentosa, RPGR, Anxiety, Medicine, Science
الوصف: Abstract Variants in the retinitis pigmentosa GTPase regulator (RPGR) gene are responsible for the majority of X-linked retinitis pigmentosa cases, which not only affects male patients but also some heterozygous females. Vision-related disability and anxiety of patients with RPGR-associated retinal degeneration have never been explored before. This study aimed to evaluate self-reported visual function and vision-related anxiety in a Portuguese cohort of male and female patients with RPGR-associated retinal degeneration using two validated patient-reported outcome measures. Cross-sectional data of thirty-two genetically-tested patients was examined, including scores of the Michigan retinal degeneration questionnaire (MRDQ) and Michigan vision-related anxiety questionnaire. Patients were classified according to retinal phenotypes in males (M), females with male phenotype (FM), and females with radial or focal pattern. Both M and FM revealed higher rod-function and cone-function anxiety scores (p
نوع الوثيقة: article
وصف الملف: electronic resource
اللغة: English
تدمد: 2045-2322
Relation: https://doaj.org/toc/2045-2322
DOI: 10.1038/s41598-024-66170-2
URL الوصول: https://doaj.org/article/dfaeb4784cab4498b3215af36880512d
رقم الأكسشن: edsdoj.faeb4784cab4498b3215af36880512d
قاعدة البيانات: Directory of Open Access Journals
الوصف
تدمد:20452322
DOI:10.1038/s41598-024-66170-2