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Idiopathic posterior uveitis is a rare, potentially sight-threatening, ocular disease, not attributed to any specific ocular or systemic cause, characterized by focal, multifocal or diffuse non-infectious inflammation in the posterior uvea (i.e. choroiditis, chorioretinitis, retinitis and neuroretinitis). Visual morbidity due to complications (including cystoid macular edema and choroidal neovascularization) has been reported.
Biomarker and diagnostic research for idiopathic posterior uveitis has been reported in the published literature.
No clinical trials have been registered for idiopathic posterior uveitis.
5 publications have been identified in PubMed for idiopathic posterior uveitis. Research spans Diagnostic / Biomarker (20%), Review / Meta-Analysis (20%), and Case Report / Case Series (20%).
Shariati MM (2026). [PMID: 41581046](https://pubmed.ncbi.nlm.nih.gov/41581046/). *Indian J Ophthalmol*. [Basic Science / Preclinical]
Ma ST (2025). [PMID: 40213301](https://pubmed.ncbi.nlm.nih.gov/40213301/). *Taiwan J Ophthalmol*. [Case Report / Case Series]
Demir U (2025). [PMID: 40922304](https://pubmed.ncbi.nlm.nih.gov/40922304/). *Medicine (Baltimore)*. [Epidemiology / Natural History]
Amer M (2025). [PMID: 41268217](https://pubmed.ncbi.nlm.nih.gov/41268217/). *J Ophthalmic Vis Res*. [Review / Meta-Analysis]
Kayabasi M (2024). [PMID: 39507809](https://pubmed.ncbi.nlm.nih.gov/39507809/). *Med Hypothesis Discov Innov Ophthalmol*. [Diagnostic / Biomarker]
Data assembled from 3 of 12 sources · Last updated Sep 19, 2026, 5:23 PM UTC
European rare disease database
Genetic and Rare Diseases Info Center