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Chromosomal disorder in which (part or full) chromosome 21 is attached to another chromosome, resulting in the presence of a third copy of part of full chromosome 21 genetic material. A Robertsonian translocation is a structural chromosomal anomaly in which two acrocentric chromosomes break, resulting in the fusion of the nonhomologous chromosomes’ long arms to form a single, large chromosome.
No clinical trials have been registered for Robertsonian translocation Down syndrome.
6 publications have been identified in PubMed for Robertsonian translocation Down syndrome. Research spans Epidemiology / Natural History (67%) and Case Report / Case Series (33%).
Rajab A (2026). [PMID: 41785191](https://pubmed.ncbi.nlm.nih.gov/41785191/). *Cytogenet Genome Res*. [Epidemiology / Natural History]
Kunda S (2026). [PMID: 41939616](https://pubmed.ncbi.nlm.nih.gov/41939616/). *Cureus*. [Epidemiology / Natural History]
Ortiz-Lagunas LA (2026). [PMID: 41955674](https://pubmed.ncbi.nlm.nih.gov/41955674/). *Arch Med Res*. [Epidemiology / Natural History]
Maharjan KK (2025). [PMID: 41268009](https://pubmed.ncbi.nlm.nih.gov/41268009/). *Med J 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 2 of 12 sources · Last updated Sep 19, 2026, 9:39 PM UTC
Common questions about Robertsonian translocation Down syndrome