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An inherited retinopathy caused by bi-allelic variants in the TRPM1 gene.
No clinical trials have been registered for TRPM1-related retinopathy.
4 publications have been identified in PubMed for TRPM1-related retinopathy. Research spans Epidemiology / Natural History (50%), Review / Meta-Analysis (25%), and Case Report / Case Series (25%).
Zaslavsky K (2025). [PMID: 41342616](https://pubmed.ncbi.nlm.nih.gov/41342616/). *Invest Ophthalmol Vis Sci*. [Epidemiology / Natural History]
Kalogeropoulos D (2025). [PMID: 40824502](https://pubmed.ncbi.nlm.nih.gov/40824502/). *Int Ophthalmol*. [Review / Meta-Analysis]
Azmon R (2025). [PMID: 40935931](https://pubmed.ncbi.nlm.nih.gov/40935931/). *Eye (Lond)*. [Epidemiology / Natural History]
Cohen DC (2024). [PMID: 39109318](https://pubmed.ncbi.nlm.nih.gov/39109318/). *Am J Ophthalmol Case Rep*. [Case Report / Case Series]
Data assembled from 2 of 12 sources · Last updated Sep 20, 2026, 4:05 PM UTC
Common questions about TRPM1-related retinopathy