About Lethal polymalformative syndrome, Boissel type
Lethal polymalformative syndrome, Boissel type is a rare disease catalogued by Orphanet (ORPHA:210144). It is associated with the FTO 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 Lethal polymalformative syndrome, Boissel type trials.
Search ClinicalTrials.gov for "Lethal polymalformative syndrome, Boissel type" or filter by Orphanet code ORPHA:210144 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 Lethal polymalformative syndrome, Boissel type trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Lethal polymalformative syndrome, Boissel type. Updated daily.