The genetics of glaucoma: Disease associations, personalised risk assessment and therapeutic opportunities‐A review
Year: 2022
Type: review
Abstract: Glaucoma refers to a heterogenous group of disorders characterised by progressive loss of retinal ganglion cells and associated visual field loss. Both early-onset and adult-onset forms of the disease have a strong genetic component. Here, we summarise the known genetic associations for various forms of glaucoma and the possible functional roles for these genes in disease pathogenesis. We also discuss efforts to translate genetic knowledge into clinical practice, including gene-based tests for disease diagnosis and risk-stratification as well as gene-based therapies.
DOI: 10.1111/ceo.14035
Authors: Inas F. Aboobakar, Janey L. Wiggs
Institutions: Massachusetts Eye and Ear Infirmary, Harvard University
Language: English
Subfield: Ophthalmology
Field: Medicine
Domain: Health Sciences
Open Access status: green
Funder: National Eye Institute
OpenAlex ID: W4205927983
