About Temple syndrome due to paternal 14q32.2 hypomethylation
Temple syndrome due to paternal 14q32.2 hypomethylation is a rare disease catalogued by Orphanet (ORPHA:254531). It is associated with the RTL1, MEG3, DLK1 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 Temple syndrome due to paternal 14q32.2 hypomethylation trials.
Search ClinicalTrials.gov for "Temple syndrome due to paternal 14q32.2 hypomethylation" or filter by Orphanet code ORPHA:254531 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 Temple syndrome due to paternal 14q32.2 hypomethylation trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Temple syndrome due to paternal 14q32.2 hypomethylation. Updated daily.