About Neurodevelopmental delay-intellectual disability-ataxia-feeding difficulty syndrome
Neurodevelopmental delay-intellectual disability-ataxia-feeding difficulty syndrome is a rare disease catalogued by Orphanet (ORPHA:647788). It is associated with the DHX30 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 Neurodevelopmental delay-intellectual disability-ataxia-feeding difficulty syndrome trials.
Search ClinicalTrials.gov for "Neurodevelopmental delay-intellectual disability-ataxia-feeding difficulty syndrome" or filter by Orphanet code ORPHA:647788 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 Neurodevelopmental delay-intellectual disability-ataxia-feeding difficulty syndrome trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Neurodevelopmental delay-intellectual disability-ataxia-feeding difficulty syndrome. Updated daily.