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An inherited retinopathy caused by bi-allelic variants in the PCARE gene.
No clinical trials have been registered for PCARE-related retinopathy.
3 publications have been identified in PubMed for PCARE-related retinopathy. Research spans Epidemiology / Natural History (67%) and Basic Science / Preclinical (33%).
Marta A (2025). [PMID: 39939324](https://pubmed.ncbi.nlm.nih.gov/39939324/). *NPJ Genom Med*. [Epidemiology / Natural History]
Bianco L (2025). [PMID: 40261664](https://pubmed.ncbi.nlm.nih.gov/40261664/). *Invest Ophthalmol Vis Sci*. [Epidemiology / Natural History]
De Geer K (2025). [PMID: 39643591](https://pubmed.ncbi.nlm.nih.gov/39643591/). *Acta Ophthalmol*. [Basic Science / Preclinical]
Data assembled from 2 of 12 sources · Last updated Sep 20, 2026, 11:13 AM UTC
Common questions about PCARE-related retinopathy