About Familial infantile bilateral striatal necrosis
Familial infantile bilateral striatal necrosis is a rare disease catalogued by Orphanet (ORPHA:225154). It is associated with the NUP54, ADAR, MT-ATP6 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 Familial infantile bilateral striatal necrosis trials.
Search ClinicalTrials.gov for "Familial infantile bilateral striatal necrosis" or filter by Orphanet code ORPHA:225154 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 Familial infantile bilateral striatal necrosis trials
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