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An inherited retinopathy caused by bi-allelic variants in the EYS gene.
No clinical trials have been registered for EYS-related retinopathy.
7 publications have been identified in PubMed for EYS-related retinopathy. Research spans Basic Science / Preclinical (43%), Case Report / Case Series (29%), and Review / Meta-Analysis (14%).
Wang Z (2026). [PMID: 41700794](https://pubmed.ncbi.nlm.nih.gov/41700794/). *Transl Vis Sci Technol*. [Basic Science / Preclinical]
Sakai D (2025). [PMID: 40989003](https://pubmed.ncbi.nlm.nih.gov/40989003/). *Front Ophthalmol (Lausanne)*. [Basic Science / Preclinical]
Marques JP (2025). [PMID: 40819709](https://pubmed.ncbi.nlm.nih.gov/40819709/). *Prog Retin Eye Res*. [Review / Meta-Analysis]
Hughes MJ (2025). [PMID: 40879293](https://pubmed.ncbi.nlm.nih.gov/40879293/). *Invest Ophthalmol Vis Sci*. [Epidemiology / Natural History]
Pongpaksupasin P (2024). [PMID: 38810502](https://pubmed.ncbi.nlm.nih.gov/38810502/). *Stem Cell Res*. [Basic Science / Preclinical]
Ruiz-Justiz AJ (2024). [PMID: 39588395](https://pubmed.ncbi.nlm.nih.gov/39588395/). *Cureus*. [Case Report / Case Series]
Data assembled from 2 of 12 sources · Last updated Sep 20, 2026, 5:49 AM UTC
Common questions about EYS-related retinopathy