About 17q24.2 microdeletion syndrome
17q24.2 microdeletion syndrome is a rare disease catalogued by Orphanet (ORPHA:529962). It is associated with the BPTF, PSMD12 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 17q24.2 microdeletion syndrome trials.
Search ClinicalTrials.gov for "17q24.2 microdeletion syndrome" or filter by Orphanet code ORPHA:529962 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 17q24.2 microdeletion syndrome trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for 17q24.2 microdeletion syndrome. Updated daily.