About Silver-Russell syndrome due to 11p15 microduplication
Silver-Russell syndrome due to 11p15 microduplication is a rare disease catalogued by Orphanet (ORPHA:231144). It is associated with the H19, IGF2 genes. 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.
Clinical Trial Eligibility Tips
What to know before applying to Silver-Russell syndrome due to 11p15 microduplication trials.
Search ClinicalTrials.gov for "Silver-Russell syndrome due to 11p15 microduplication" or filter by Orphanet code ORPHA:231144 to find disease-specific studies.
Ask your specialist to refer you to a Centre of Expertise — Orphanet lists all accredited centres for this condition worldwide.
Natural history studies and patient registries often enrol before drug trials open — contact the Orphanet patient community first.
Patient Resources
Find recruiting Silver-Russell syndrome due to 11p15 microduplication trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Silver-Russell syndrome due to 11p15 microduplication. Updated daily.