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Cataract-microcornea syndrome is characterized by the association of congenital cataract and microcornea without any other systemic anomaly or dysmorphism.
Estimated prevalence: Unknown (Unknown prevalence).
No clinical trials have been registered for cataract - microcornea syndrome.
5 publications have been identified in PubMed for cataract - microcornea syndrome. Research spans Case Report / Case Series (60%), Review / Meta-Analysis (20%), and Basic Science / Preclinical (20%).
Kang S (2026). [PMID: 41236190](https://pubmed.ncbi.nlm.nih.gov/41236190/). *Ophthalmic genetics*. [Case Report / Case Series]
Huang T (2026). [PMID: 41822754](https://pubmed.ncbi.nlm.nih.gov/41822754/). *Frontiers in genetics*. [Basic Science / Preclinical]
Kesimal B (2025). [PMID: 41189786](https://pubmed.ncbi.nlm.nih.gov/41189786/). *Romanian journal of ophthalmology*. [Case Report / Case Series]
Chandran KR (2025). [PMID: 40125772](https://pubmed.ncbi.nlm.nih.gov/40125772/). *Journal of pediatric ophthalmology and strabismus*. [Case Report / Case Series]
Luo NC (2025). [PMID: 40302600](https://pubmed.ncbi.nlm.nih.gov/40302600/). *[Zhonghua yan ke za zhi] Chinese journal of ophthalmology*. [Review / Meta-Analysis]
Data assembled from 3 of 12 sources · Last updated Sep 19, 2026, 12:50 AM UTC
European rare disease database
Genetic and Rare Diseases Info Center