About Severe neonatal lactic acidosis due to NFS1-ISD11 complex deficiency
Severe neonatal lactic acidosis due to NFS1-ISD11 complex deficiency is a rare disease catalogued by Orphanet (ORPHA:397593). It is associated with the LYRM4, NFS1 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 Severe neonatal lactic acidosis due to NFS1-ISD11 complex deficiency trials.
Search ClinicalTrials.gov for "Severe neonatal lactic acidosis due to NFS1-ISD11 complex deficiency" or filter by Orphanet code ORPHA:397593 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 Severe neonatal lactic acidosis due to NFS1-ISD11 complex deficiency trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Severe neonatal lactic acidosis due to NFS1-ISD11 complex deficiency. Updated daily.