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Chromosome 8p deletion is a chromosome abnormality that affects many different parts of the body. People with this condition are missing genetic material located on the short arm (p) of chromosome 8 in each cell. The severity of the condition and the associated signs and symptoms vary based on the size and location of the deletion and which genes are involved. Most cases are not inherited, although affected people can pass the deletion on to their children. Treatment is based on the signs and symptoms present in each person.
Biomarker and diagnostic research for partial deletion of the short arm of chromosome 8 has been reported in the published literature.
No clinical trials have been registered for partial deletion of the short arm of chromosome 8.
12 publications have been identified in PubMed for partial deletion of the short arm of chromosome 8. Research spans Basic Science / Preclinical (33%), Diagnostic / Biomarker (17%), and Case Report / Case Series (17%).
Research Type | Count | % of Total |
|---|---|---|
Laboratory research | 4 | 33% |
Data assembled from 3 of 12 sources · Last updated Sep 19, 2026, 11:16 PM UTC
European rare disease database
Genetic and Rare Diseases Info Center
Testing and diagnosis research
2 |
17% |
Patient case studies | 2 | 17% |
Research summaries | 1 | 8% |
Clinical study results | 1 | 8% |
Disease patterns and progression | 1 | 8% |
New treatment approaches | 1 | 8% |
Saakyan SV (2026). [PMID: 41847805](https://pubmed.ncbi.nlm.nih.gov/41847805/). *Vestn Oftalmol*. [Epidemiology / Natural History]
Hou J (2026). [PMID: 41690476](https://pubmed.ncbi.nlm.nih.gov/41690476/). *Mod Pathol*. [Basic Science / Preclinical]
Jovanovic D (2025). [PMID: 40693640](https://pubmed.ncbi.nlm.nih.gov/40693640/). *Acta Med Acad*. [Case Report / Case Series]
Kahr J (2025). [PMID: 39969396](https://pubmed.ncbi.nlm.nih.gov/39969396/). *Clin Neuropathol*. [Case Report / Case Series]
Yang X (2025). [PMID: 40790240](https://pubmed.ncbi.nlm.nih.gov/40790240/). *Orphanet J Rare Dis*. [Basic Science / Preclinical]
Hayashi M (2025). [PMID: 39894565](https://pubmed.ncbi.nlm.nih.gov/39894565/). *Biomed Res*. [Basic Science / Preclinical]
Horbacz M (2025). [PMID: 41210864](https://pubmed.ncbi.nlm.nih.gov/41210864/). *Front Med (Lausanne)*. [Diagnostic / Biomarker]
Santucci K (2025). [PMID: 39390634](https://pubmed.ncbi.nlm.nih.gov/39390634/). *Clin Genet*. [Review / Meta-Analysis]
Zhou C (2024). [PMID: 40406282](https://pubmed.ncbi.nlm.nih.gov/40406282/). *Matern Fetal Med*. [Diagnostic / Biomarker]
Krieg S (2024). [PMID: 38886830](https://pubmed.ncbi.nlm.nih.gov/38886830/). *Genome Med*. [Gene Therapy / Novel Therapeutics]