Rare condition
Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15
0
studies recruiting now
as of 7 Sept 2026
0
studies registered in total
as of 7 Sept 2026
0
countries with a recruiting site
as of 7 Sept 2026
None
recruiting study posted to date
among recruiting studies
Recruiting trials
No registered studies found for Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15.
ClinicalTrials.gov has no study listed under this name as of 7 Sept 2026. That can change, and there are other routes worth knowing about.
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Patient organisations
We do not yet list a dedicated organisation for this condition. The directories below are the best route.
About Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15
RareTrial does not yet hold a plain-language description of this condition. The most reliable starting point is Orphanet’s expert page, which lists specialist centres, registries and patient organisations, and the genes involved (SNRPN, MAGEL2, NDN, OCA2).
Treatments being studied
1 approved treatment and 16 in clinical development, from Open Targets (CC BY 4.0). Not medical advice.
+ 8 more in development
Related conditions
Information, not medical advice. Trial listings are shown as recorded on ClinicalTrials.gov; whether any study is right for you is a decision for you and your clinicians, and eligibility is decided by each research team. Disease information from Orphanet (CC BY 4.0).