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Accessory tricuspid valve tissue is a rare, congenital, atrioventricular valve malformation characterized by fixed or mobile accessory tissue on the tricuspid valve, usually associated with other complex congenital heart anomalies (atrial septal defect, ventricular septal defect, transposition of great arteries, tetralogy Fallot). It may present clinically with systolic murmur, dyspnea, cyanosis, depending also on accompanying congenital heart anomaly.
No clinical trials have been registered for accessory tricuspid valve tissue.
3 publications have been identified in PubMed for accessory tricuspid valve tissue. Research spans Case Report / Case Series (67%) and Other (33%).
Maruyama A (2026). [PMID: 42148255](https://pubmed.ncbi.nlm.nih.gov/42148255/). *Eur Heart J Case Rep*. [Case Report / Case Series]
Ahmed A (2025). [PMID: 40250907](https://pubmed.ncbi.nlm.nih.gov/40250907/). *JACC Case Rep*. [Case Report / Case Series]
Sakamoto A (2025). [PMID: 40250944](https://pubmed.ncbi.nlm.nih.gov/40250944/). *JACC Case Rep*. [Other]
Data assembled from 3 of 12 sources · Last updated Sep 19, 2026, 1:55 PM UTC
European rare disease database
Genetic and Rare Diseases Info Center
Common questions about accessory tricuspid valve tissue