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Biomarker and diagnostic research for Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15 has been reported in the published literature.
No clinical trials have been registered for Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15.
11 publications have been identified in PubMed for Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15. Research spans Case Report / Case Series (45%), Review / Meta-Analysis (27%), and Diagnostic / Biomarker (18%).
Research Type | Count | % of Total |
|---|---|---|
Patient case studies | 5 | 45% |
Data assembled from 3 of 12 sources · Last updated Oct 4, 2026, 12:42 AM UTC
European rare disease database
Genetic and Rare Diseases Info Center
Common questions about Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15
Research summaries |
3 |
27% |
Testing and diagnosis research | 2 | 18% |
Clinical study results | 1 | 9% |
Śledzikowska Z (2026). [PMID: 41677631](https://pubmed.ncbi.nlm.nih.gov/41677631/). *Cells*. [Review / Meta-Analysis]
Xue S (2026). [PMID: 41118657](https://pubmed.ncbi.nlm.nih.gov/41118657/). *Ultrasound Obstet Gynecol*. [Review / Meta-Analysis]
Marczyk T (2025). [PMID: 40565581](https://pubmed.ncbi.nlm.nih.gov/40565581/). *Genes (Basel)*. [Case Report / Case Series]
Gigonzac TCV (2025). [PMID: 40943430](https://pubmed.ncbi.nlm.nih.gov/40943430/). *Int J Mol Sci*. [Case Report / Case Series]
Martínez JB (2025). [PMID: 40200592](https://pubmed.ncbi.nlm.nih.gov/40200592/). *Clin Genet*. [Case Report / Case Series]
Ye Y (2025). [PMID: 41244984](https://pubmed.ncbi.nlm.nih.gov/41244984/). *Front Genet*. [Diagnostic / Biomarker]
Nannan Y (2025). [PMID: 40883760](https://pubmed.ncbi.nlm.nih.gov/40883760/). *Mol Cytogenet*. [Case Report / Case Series]
Schmok T (2024). [PMID: 38837660](https://pubmed.ncbi.nlm.nih.gov/38837660/). *Am J Med Genet A*. [Clinical Trial Publication]
Petersson M (2024). [PMID: 39194735](https://pubmed.ncbi.nlm.nih.gov/39194735/). *Curr Issues Mol Biol*. [Review / Meta-Analysis]
Janssen EJM (2024). [PMID: 38747584](https://pubmed.ncbi.nlm.nih.gov/38747584/). *Ned Tijdschr Geneeskd*. [Case Report / Case Series]