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Estimated prevalence: <1 in 1,000,000 (VERY_RARE).
No clinical trials have been registered for foveal hypoplasia-presenile cataract syndrome.
10 publications have been identified in PubMed for foveal hypoplasia-presenile cataract syndrome. Research spans Case Report / Case Series (60%), Review / Meta-Analysis (20%), and Basic Science / Preclinical (10%).
Research Type | Count | % of Total |
|---|---|---|
Patient case studies | 6 | 60% |
Data assembled from 3 of 12 sources · Last updated Sep 20, 2026, 4:39 PM UTC
European rare disease database
Genetic and Rare Diseases Info Center
Research summaries
2 |
20% |
Laboratory research | 1 | 10% |
Disease patterns and progression | 1 | 10% |
Lang B (2026). [PMID: 41898295](https://pubmed.ncbi.nlm.nih.gov/41898295/). *Biomedicines*. [Case Report / Case Series]
Arcot Sadagopan K (2025). [PMID: 40083070](https://pubmed.ncbi.nlm.nih.gov/40083070/). *Ophthalmic genetics*. [Case Report / Case Series]
Mesquita R (2025). [PMID: 40725401](https://pubmed.ncbi.nlm.nih.gov/40725401/). *Genes*. [Epidemiology / Natural History]
Urzua CA (2025). [PMID: 40082704](https://pubmed.ncbi.nlm.nih.gov/40082704/). *Eye (London, England)*. [Case Report / Case Series]
Beresford-Webb JA (2025). [PMID: 40134611](https://pubmed.ncbi.nlm.nih.gov/40134611/). *Journal of ophthalmology*. [Review / Meta-Analysis]
Hall J (2025). [PMID: 40138169](https://pubmed.ncbi.nlm.nih.gov/40138169/). *Ophthalmology and therapy*. [Review / Meta-Analysis]
Zhong A (2025). [PMID: 40140649](https://pubmed.ncbi.nlm.nih.gov/40140649/). *Ophthalmic genetics*. [Basic Science / Preclinical]
Van Haecke H (2025). [PMID: 40545376](https://pubmed.ncbi.nlm.nih.gov/40545376/). *Ophthalmic genetics*. [Case Report / Case Series]
Szeligowski T (2024). [PMID: 39336769](https://pubmed.ncbi.nlm.nih.gov/39336769/). *Genes*. [Case Report / Case Series]
Fan J (2024). [PMID: 38699441](https://pubmed.ncbi.nlm.nih.gov/38699441/). *American journal of ophthalmology case reports*. [Case Report / Case Series]