About Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome
Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome is a rare disease catalogued by Orphanet (ORPHA:391408). It is associated with the PPP1R15B, TRMT10A 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 Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome trials.
Search ClinicalTrials.gov for "Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome" or filter by Orphanet code ORPHA:391408 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 Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Primary microcephaly-mild intellectual disability-young-onset diabetes syndrome. Updated daily.