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A syndrome characterized by postlingual progressive hearing loss, abnormalities in the vestibular system, and onset of retinitis pigmentosa symptoms usually by the second decade of life.
Estimated prevalence: 1-9 in 1,000,000 (Rare).
1 clinical trial registered. Interventions under study include drug therapy. Pipeline includes 1 PHASE1. Research is primarily sponsored by academic and government institutions.
6 publications have been identified in PubMed for Usher syndrome type 3. Research spans Epidemiology / Natural History (50%), Review / Meta-Analysis (17%), and Case Report / Case Series (17%).
Siu VM (2026). [PMID: 42157369](https://pubmed.ncbi.nlm.nih.gov/42157369/). *Am J Med Genet A*. [Gene Therapy / Novel Therapeutics]
Zhang H (2025). [PMID: 39487674](https://pubmed.ncbi.nlm.nih.gov/39487674/). *IUBMB life*. [Review / Meta-Analysis]
Rogic S (2025). [PMID: 40719025](https://pubmed.ncbi.nlm.nih.gov/40719025/). *Disease models & mechanisms*. [Epidemiology / Natural History]
Cromar ZJ (2025). [PMID: 40533831](https://pubmed.ncbi.nlm.nih.gov/40533831/). *Human genomics*. [Epidemiology / Natural History]
Alkan AA (2025). [PMID: 41200749](https://pubmed.ncbi.nlm.nih.gov/41200749/). *The Journal of international medical research*. [Epidemiology / Natural History]
Data assembled from 4 of 12 sources · Last updated Sep 18, 2026, 7:14 PM UTC
European rare disease database
Genetic and Rare Diseases Info Center
Common questions about Usher syndrome type 3
Wang S (2024). [PMID: 39304915](https://pubmed.ncbi.nlm.nih.gov/39304915/). *Orphanet journal of rare diseases*. [Case Report / Case Series]