About Multiple congenital anomalies-neurodevelopmental delay-ocular abnormalities syndrome
Multiple congenital anomalies-neurodevelopmental delay-ocular abnormalities syndrome is a rare disease catalogued by Orphanet (ORPHA:659904). It is associated with the PRR12 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 Multiple congenital anomalies-neurodevelopmental delay-ocular abnormalities syndrome trials.
Search ClinicalTrials.gov for "Multiple congenital anomalies-neurodevelopmental delay-ocular abnormalities syndrome" or filter by Orphanet code ORPHA:659904 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 Multiple congenital anomalies-neurodevelopmental delay-ocular abnormalities syndrome trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Multiple congenital anomalies-neurodevelopmental delay-ocular abnormalities syndrome. Updated daily.