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Idiopathic panuveitis is a rare inflammatory eye disease, of unknown etiology, characterized by generalized inflammation of the uvea (iris, ciliary body, choroid), retina and vitreous with consequent ciliary spasm and posterior synechiae formation, leading to acute or chronic, unilateral or bilateral visual impairment and ocular discomfort or pain. Patients present an increased risk of development of cataracts, secondary glaucoma, cystoid macular edema and/or retinal detachment. It could potentially result in vision loss.
Estimated prevalence: 1-9 in 100,000 (Uncommon).
No clinical trials have been registered for idiopathic panuveitis.
5 publications have been identified in PubMed for idiopathic panuveitis. Research spans Case Report / Case Series (80%) and Epidemiology / Natural History (20%).
Burggraaf-Sánchez de Las Matas R (2025). [PMID: 41112496](https://pubmed.ncbi.nlm.nih.gov/41112496/). *Journal of vitreoretinal diseases*. [Case Report / Case Series]
Guo K (2025). [PMID: 40515519](https://pubmed.ncbi.nlm.nih.gov/40515519/). *Ocular immunology and inflammation*. [Case Report / Case Series]
Nguyen AT (2025). [PMID: 38710493](https://pubmed.ncbi.nlm.nih.gov/38710493/). *Rheumatology (Oxford, England)*. [Epidemiology / Natural History]
Konda SM (2024). [PMID: 37037028](https://pubmed.ncbi.nlm.nih.gov/37037028/). *Retinal cases & brief reports*. [Case Report / Case Series]
Tungsattayathitthan U (2024). [PMID: 38649909](https://pubmed.ncbi.nlm.nih.gov/38649909/). *BMC ophthalmology*. [Case Report / Case Series]
Data assembled from 3 of 12 sources · Last updated Sep 20, 2026, 2:11 PM UTC
European rare disease database
Genetic and Rare Diseases Info Center