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Estimated prevalence: <1 in 1,000,000 (VERY_RARE).
No clinical trials have been registered for congenital retinal arteriovenous communication.
3 publications have been identified in PubMed for congenital retinal arteriovenous communication. Research spans Case Report / Case Series (100%).
Wong TH (2026). [PMID: 42017869](https://pubmed.ncbi.nlm.nih.gov/42017869/). *Ophthalmol Retina*. [Case Report / Case Series]
Wu C (2025). [PMID: 40545013](https://pubmed.ncbi.nlm.nih.gov/40545013/). *American journal of ophthalmology*. [Case Report / Case Series]
Hupin N (2024). [PMID: 39669759](https://pubmed.ncbi.nlm.nih.gov/39669759/). *American journal of ophthalmology case reports*. [Case Report / Case Series]
Data assembled from 3 of 12 sources · Last updated Sep 20, 2026, 4:05 PM UTC
European rare disease database
Genetic and Rare Diseases Info Center