Rare condition
Angelman syndrome due to maternal 15q11q13 deletion
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 Angelman syndrome due to maternal 15q11q13 deletion.
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.
Keep watching
Get an email when a new Angelman syndrome due to maternal 15q11q13 deletion study opens.
One email a day at most. Unsubscribe with one click.
Used only for these alerts. Privacy.
Support
Patient organisations
We do not yet list a dedicated organisation for this condition. The directories below are the best route.
About Angelman syndrome due to maternal 15q11q13 deletion
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 (UBE3A, OCA2).
Treatments being studied
8 in clinical development, from Open Targets (CC BY 4.0). Not medical advice.
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).