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Trisomy 10p is a syndrome of mental retardation/multiple congenital malformations (MR-MCA) that is caused by the total or partial duplication of the short arm of chromosome 10.
Estimated prevalence: Unknown (Unknown prevalence).
No clinical trials have been registered for trisomy 10p.
3 publications have been identified in PubMed for trisomy 10p. Research spans Basic Science / Preclinical (67%) and Case Report / Case Series (33%).
Vormittag-Nocito E (2025). [PMID: 40239807](https://pubmed.ncbi.nlm.nih.gov/40239807/). *Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc*. [Basic Science / Preclinical]
Fan F (2025). [PMID: 41811051](https://pubmed.ncbi.nlm.nih.gov/41811051/). *Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics*. [Case Report / Case Series]
Nair NU (2024). [PMID: 39078448](https://pubmed.ncbi.nlm.nih.gov/39078448/). *Cancer research*. [Basic Science / Preclinical]
Data assembled from 3 of 12 sources · Last updated Sep 18, 2026, 7:12 PM UTC
European rare disease database
Genetic and Rare Diseases Info Center