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Any retinopathy caused by a variant in the RHO gene, including cases diagnosed as congenital stationary night blindness autosomal dominant 1 or retinitis pigmentosa 4.
No clinical trials have been registered for RHO-related retinopathy.
6 publications have been identified in PubMed for RHO-related retinopathy. Research spans Review / Meta-Analysis (50%), Basic Science / Preclinical (33%), and Epidemiology / Natural History (17%).
Nakamura N (2026). [PMID: 41762300](https://pubmed.ncbi.nlm.nih.gov/41762300/). *J Neurol*. [Epidemiology / Natural History]
Ye Y (2026). [PMID: 41963275](https://pubmed.ncbi.nlm.nih.gov/41963275/). *J Ocul Pharmacol Ther*. [Basic Science / Preclinical]
Tan JK (2025). [PMID: 40250716](https://pubmed.ncbi.nlm.nih.gov/40250716/). *Surv Ophthalmol*. [Review / Meta-Analysis]
Wong WM (2025). [PMID: 40013354](https://pubmed.ncbi.nlm.nih.gov/40013354/). *Clin Exp Ophthalmol*. [Review / Meta-Analysis]
Tebbe L (2024). [PMID: 38799985](https://pubmed.ncbi.nlm.nih.gov/38799985/). *Front Cell Neurosci*. [Review / Meta-Analysis]
Data assembled from 2 of 12 sources · Last updated Oct 3, 2026, 3:53 PM UTC
Common questions about RHO-related retinopathy