About Childhood-onset spasticity with hyperglycinemia
Childhood-onset spasticity with hyperglycinemia is a rare disease catalogued by Orphanet (ORPHA:401866). It is associated with the GLRX5 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 Childhood-onset spasticity with hyperglycinemia trials.
Search ClinicalTrials.gov for "Childhood-onset spasticity with hyperglycinemia" or filter by Orphanet code ORPHA:401866 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 Childhood-onset spasticity with hyperglycinemia trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Childhood-onset spasticity with hyperglycinemia. Updated daily.