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A rare eyelid malposition disorder characterized by congenital abnormal inversion of the eyelid towards the globe, potentially causing mechanical irritation of the ocular surface by the eyelashes, which may lead to corneal abrasion and scarring with visual impairment. Typical initial symptoms are foreign body sensation, redness, tearing, and ocular discharge.
No clinical trials have been registered for isolated congenital entropion.
1 publication has been identified in PubMed for isolated congenital entropion. Research spans Review / Meta-Analysis (100%).
Peyman A (2024). [PMID: 38709200](https://pubmed.ncbi.nlm.nih.gov/38709200/). *Ocul Immunol Inflamm*. [Review / Meta-Analysis]
Data assembled from 3 of 12 sources · Last updated Sep 19, 2026, 2:58 PM UTC
European rare disease database
Genetic and Rare Diseases Info Center