About 3-phosphoserine phosphatase deficiency, infantile/juvenile form
3-phosphoserine phosphatase deficiency, infantile/juvenile form is a rare disease catalogued by Orphanet (ORPHA:79350). It is associated with the PSPH 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 3-phosphoserine phosphatase deficiency, infantile/juvenile form trials.
Search ClinicalTrials.gov for "3-phosphoserine phosphatase deficiency, infantile/juvenile form" or filter by Orphanet code ORPHA:79350 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 3-phosphoserine phosphatase deficiency, infantile/juvenile form trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for 3-phosphoserine phosphatase deficiency, infantile/juvenile form. Updated daily.