Prevention and early intervention screening for inherited ocular diseases in Saudi Arabia: a national perspective
Mariam M. AlEissa, Malak Abedalthagafi, Deepak P. Edward

TL;DR
This paper discusses the need for national screening programs to prevent and manage inherited eye diseases in Saudi Arabia due to high rates of consanguineous marriages.
Contribution
The paper proposes a national framework for early intervention and screening of inherited ocular diseases in Saudi Arabia.
Findings
High rates of consanguineous marriages increase the risk of inherited ocular diseases in Saudi Arabia.
Early genetic screening and counseling can reduce long-term healthcare costs and improve health outcomes.
Telemedicine and AI tools can enhance accessibility and accuracy in screening programs.
Abstract
Consanguineous marriages are common, particularly in Saudi Arabia, where approximately half of all marriages are consanguineous. The likelihood of autosomal recessive (AR) genetic abnormalities, especially rare diseases (RDs) that present long-term health issues, is significantly increased by this trend, making Inherited Ocular Diseases (IODs) a public health concern in Saudi Arabia. The common IODs include Primary Congenital Glaucoma (PCG), Retinitis Pigmentosa (RP), and Leber Congenital Amaurosis (LCA). To date, there are no national initiatives for screening programs to detect, prevent, and manage IOD. This review aims to evaluate the public health landscape of IOD in Saudi Arabia, including epidemiology and genetic factors. It highlights the need for a national framework to facilitate screening, prevention, and early intervention. Cost-effectiveness evaluation, early genetic…
Genes, proteins, chemicals, diseases, species, mutations and cell lines named across the full text — each resolved to its canonical identifier and authoritative record.
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Taxonomy
TopicsGenomics and Rare Diseases · Ophthalmology and Visual Impairment Studies · Glaucoma and retinal disorders
