About Prader-Willi syndrome due to paternal 15q11q13 deletion
Prader-Willi syndrome due to paternal 15q11q13 deletion is a rare disease catalogued by Orphanet (ORPHA:98793). Search below for active recruiting clinical trials from ClinicalTrials.gov, or visit the Orphanet expert page for specialist centres, natural history studies, and patient registries worldwide.
Clinical Trial Eligibility Tips
What to know before applying to Prader-Willi syndrome due to paternal 15q11q13 deletion trials.
Search ClinicalTrials.gov for "Prader-Willi syndrome due to paternal 15q11q13 deletion" or Orphanet code ORPHA:98793 to find disease-specific recruiting studies.
Ask your specialist to refer you to an Orphanet-accredited Centre of Expertise for this condition.
Natural history studies and patient registries often open enrolment before drug trials — contact the Orphanet patient community first.
Patient Resources
Find recruiting Prader-Willi syndrome due to paternal 15q11q13 deletion trials
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