About Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7
Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7 is a rare disease catalogued by Orphanet (ORPHA:96182). It is associated with the GRB10 gene. 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 maternal uniparental disomy of chromosome 7 trials.
Search ClinicalTrials.gov for "Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7" or filter by Orphanet code ORPHA:96182 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 maternal uniparental disomy of chromosome 7 trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Silver-Russell syndrome due to maternal uniparental disomy of chromosome 7. Updated daily.