The socioeconomic epidemiology of inherited retinal diseases in Portugal

Bibliographic Details
Title: The socioeconomic epidemiology of inherited retinal diseases in Portugal
Authors: Ana Marta, João Pedro Marques, Cristina Santos, Luísa Coutinho-Santos, Sara Vaz-Pereira, José Costa, Pedro Arede, Raquel Félix, Sara Geada, Nuno Gouveia, Rui Silva, Margarida Baptista, Miguel Lume, Ricardo Parreira, Célia Azevedo Soares, Maria João Menéres, Carolina Lemos, João Melo Beirão
Source: Orphanet Journal of Rare Diseases, Vol 19, Iss 1, Pp 1-12 (2024)
Publisher Information: BMC, 2024.
Publication Year: 2024
Collection: LCC:Medicine
Subject Terms: Inherited retinal diseases, Epidemiology, Economics, Social, Medicine
More Details: Abstract Background Inherited retinal diseases (IRDs) are a group of rare degenerative disorders of the retina that can lead to blindness from birth to late middle age. Knowing the target population and its resources is essential to better plan support measures. The aim of this study was to evaluate the socioeconomic characteristics of regions in Portugal where IRD patients reside to inform the planning of vision aid and rehabilitation intervention measures. Results This study included 1082 patients from 973 families, aged 3 to 92 years, with a mean age of 44.8 ± 18.1 years. Patients living with an IRD were identified in 190 of the 308 municipalities. According to this study, the estimated IRD prevalence in Portugal was 10.4 per 100,000 inhabitants, and by municipalities, it ranged from 0 to 131.2 per 100,000 inhabitants. Overall, regions with a higher prevalence of IRD have a lower population density (r=-0.371, p
Document Type: article
File Description: electronic resource
Language: English
ISSN: 1750-1172
Relation: https://doaj.org/toc/1750-1172
DOI: 10.1186/s13023-024-03161-6
Access URL: https://doaj.org/article/9875a6d3f0cd430c869ea987bc399996
Accession Number: edsdoj.9875a6d3f0cd430c869ea987bc399996
Database: Directory of Open Access Journals
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More Details
ISSN:17501172
DOI:10.1186/s13023-024-03161-6
Published in:Orphanet Journal of Rare Diseases
Language:English