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- W3134733170 endingPage "288" @default.
- W3134733170 startingPage "270" @default.
- W3134733170 abstract "Abstract Inherited retinal diseases (IRDs) are a clinically and genetically heterogeneous group of disorders characterised by photoreceptor degeneration or dysfunction. These disorders typically present with severe vision loss that can be progressive, with disease onset ranging from congenital to late adulthood. The advances in genetics, retinal imaging and molecular biology, have conspired to create the ideal environment for establishing treatments for IRDs, with the first approved gene therapy and the commencement of multiple clinical trials. The scope of this review is to familiarise clinicians and scientists with the current management and the prospects for novel therapies for: (1) macular dystrophies, (2) cone and cone‐rod dystrophies, (3) cone dysfunction syndromes, (4) Leber congenital amaurosis, (5) rod‐cone dystrophies, (6) rod dysfunction syndromes and (7) chorioretinal dystrophies. We also briefly summarise the investigated end points for the ongoing trials." @default.
- W3134733170 created "2021-03-15" @default.
- W3134733170 creator A5015985989 @default.
- W3134733170 creator A5070277537 @default.
- W3134733170 creator A5077508604 @default.
- W3134733170 date "2021-03-20" @default.
- W3134733170 modified "2023-10-17" @default.
- W3134733170 title "Inherited retinal diseases: Therapeutics, clinical trials and end points—A review" @default.
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