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Cerulean cataract is a type of hereditary congenital cataract distinguished by bluish and white opacifications in the superficial layers of the fetal lens nucleus and adult lens nucleus and characterized by reduced visual acuity in childhood, eventually necessitating extraction of the lens.
No clinical trials have been registered for cerulean cataract.
6 publications have been identified in PubMed for cerulean cataract. Research spans Case Report / Case Series (83%) and Review / Meta-Analysis (17%).
Taklit O (2026). [PMID: 41780093](https://pubmed.ncbi.nlm.nih.gov/41780093/). *J Fr Ophtalmol*. [Case Report / Case Series]
Przysiezny B (2026). [PMID: 41987496](https://pubmed.ncbi.nlm.nih.gov/41987496/). *Ophthalmic Genet*. [Case Report / Case Series]
Dev V (2025). [PMID: 40903098](https://pubmed.ncbi.nlm.nih.gov/40903098/). *BMJ Case Rep*. [Case Report / Case Series]
Kasturi N (2025). [PMID: 40330968](https://pubmed.ncbi.nlm.nih.gov/40330968/). *Rom J Ophthalmol*. [Case Report / Case Series]
Shiels A (2024). [PMID: 38927721](https://pubmed.ncbi.nlm.nih.gov/38927721/). *Genes (Basel)*. [Review / Meta-Analysis]
Britz L (2024). [PMID: 38528250](https://pubmed.ncbi.nlm.nih.gov/38528250/). *Ophthalmologie*. [Case Report / Case Series]
Data assembled from 3 of 12 sources · Last updated Oct 10, 2026, 5:22 PM UTC
European rare disease database
Genetic and Rare Diseases Info Center