Kisho is an information platform, not a medical provider. Nothing on this site constitutes medical advice, diagnosis, or treatment recommendations. All content is aggregated from publicly available sources (including ClinicalTrials.gov, PubMed, FDA.gov, and Orphanet) and is provided for informational purposes only. Clinical trial eligibility, treatment decisions, and any health-related actions should always be discussed with a qualified healthcare professional. Kisho does not endorse any specific therapy, organization, or clinical trial. Terms of use · Privacy policy
A cytogenetic abnormality that refers to the allelic loss of all or part of the short arm of chromosome 12.
No clinical trials have been registered for chromosome 12p deletion.
3 publications have been identified in PubMed for chromosome 12p deletion. Research spans Review / Meta-Analysis (33%), Case Report / Case Series (33%), and Epidemiology / Natural History (33%).
Sun X (2026). [PMID: 41630262](https://pubmed.ncbi.nlm.nih.gov/41630262/). *Medicine*. [Case Report / Case Series]
Privitera F (2026). [PMID: 41595523](https://pubmed.ncbi.nlm.nih.gov/41595523/). *Genes*. [Review / Meta-Analysis]
Paprocka J (2024). [PMID: 38837855](https://pubmed.ncbi.nlm.nih.gov/38837855/). *Epilepsia open*. [Epidemiology / Natural History]
Data assembled from 3 of 12 sources · Last updated Sep 20, 2026, 12:38 AM UTC
European rare disease database
Genetic and Rare Diseases Info Center