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Down syndrome in which the extra (partial or total) copy of chromosome 21 genetic material is attached to another chromosome.
1 clinical trial registered. Interventions under study include other interventions. Research is primarily sponsored by academic and government institutions.
8 publications have been identified in PubMed for translocation Down syndrome. Research spans Epidemiology / Natural History (50%), Case Report / Case Series (25%), and Basic Science / Preclinical (25%).
Rajab A (2026). [PMID: 41785191](https://pubmed.ncbi.nlm.nih.gov/41785191/). *Cytogenetic and genome research*. [Epidemiology / Natural History]
Ortiz-Lagunas LA (2026). [PMID: 41955674](https://pubmed.ncbi.nlm.nih.gov/41955674/). *Arch Med Res*. [Epidemiology / Natural History]
Kunda S (2026). [PMID: 41939616](https://pubmed.ncbi.nlm.nih.gov/41939616/). *Cureus*. [Epidemiology / Natural History]
Maharjan KK (2025). [PMID: 41268009](https://pubmed.ncbi.nlm.nih.gov/41268009/). *Medical journal, Armed Forces India*. [Epidemiology / Natural History]
De Falco A (2024). [PMID: 38994932](https://pubmed.ncbi.nlm.nih.gov/38994932/). *Cells*. [Case Report / Case Series]
Data assembled from 3 of 12 sources · Last updated Sep 18, 2026, 1:47 PM UTC
Demirhan O (2024). [PMID: 38721584](https://pubmed.ncbi.nlm.nih.gov/38721584/). *Journal of pediatric genetics*. [Basic Science / Preclinical]
Gerton JL (2024). [PMID: 38606789](https://pubmed.ncbi.nlm.nih.gov/38606789/). *Journal of cell science*. [Basic Science / Preclinical]
Chen CP (2024). [PMID: 39482007](https://pubmed.ncbi.nlm.nih.gov/39482007/). *Taiwanese journal of obstetrics & gynecology*. [Case Report / Case Series]
AI-curated news mentioning translocation Down syndrome
Updated Sep 7, 2026
A case report highlights hepatic tuberculosis as a final diagnosis in a child with Down syndrome, initially suspected to have bartonellosis. This finding underscores the importance of considering a broad differential diagnosis in pediatric patients with complex presentations.
Recent research provides insights into rodent models of Down syndrome, highlighting their potential for translational applications. These models may enhance understanding of the disease and aid in developing therapeutic strategies.
A case report details cryptogenic multifocal ulcerating stenosing enteritis in a patient with Down syndrome, highlighting a rare gastrointestinal condition. This study contributes to the understanding of CMUSE and its implications in patients with genetic disorders.