About Intrauterine growth restriction-short stature-early adult-onset diabetes syndrome
Intrauterine growth restriction-short stature-early adult-onset diabetes syndrome is a rare disease catalogued by Orphanet (ORPHA:436144). It is associated with the CDKN1C 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 Intrauterine growth restriction-short stature-early adult-onset diabetes syndrome trials.
Search ClinicalTrials.gov for "Intrauterine growth restriction-short stature-early adult-onset diabetes syndrome" or filter by Orphanet code ORPHA:436144 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 Intrauterine growth restriction-short stature-early adult-onset diabetes syndrome trials
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