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Autosomal dominant form of rhegmatogenous retinal detachment.
Estimated prevalence: <1 in 1,000,000 (VERY_RARE).
No clinical trials have been registered for autosomal dominant rhegmatogenous retinal detachment.
3 publications have been identified in PubMed for autosomal dominant rhegmatogenous retinal detachment. Research spans Case Report / Case Series (100%).
Al-Qahtani F (2026). [PMID: 41715899](https://pubmed.ncbi.nlm.nih.gov/41715899/). *Am J Case Rep*. [Case Report / Case Series]
Kawaguchi N (2025). [PMID: 40041245](https://pubmed.ncbi.nlm.nih.gov/40041245/). *Cureus*. [Case Report / Case Series]
Choudhary A (2025). [PMID: 39544027](https://pubmed.ncbi.nlm.nih.gov/39544027/). *Eur J Ophthalmol*. [Case Report / Case Series]
Data assembled from 3 of 12 sources · Last updated Sep 19, 2026, 3:02 AM UTC
European rare disease database
Genetic and Rare Diseases Info Center
AI-curated news mentioning autosomal dominant rhegmatogenous retinal detachment
Updated May 14, 2026
A new study explores the intersection of Coats' disease and rhegmatogenous retinal detachment in adult-onset cases. This research highlights the complexities of diagnosing and treating these conditions in adults.