About Severe hypotonia-psychomotor developmental delay-strabismus-cardiac septal defect syndrome
Severe hypotonia-psychomotor developmental delay-strabismus-cardiac septal defect syndrome is a rare disease catalogued by Orphanet (ORPHA:467176). It is associated with the CCDC174 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 Severe hypotonia-psychomotor developmental delay-strabismus-cardiac septal defect syndrome trials.
Search ClinicalTrials.gov for "Severe hypotonia-psychomotor developmental delay-strabismus-cardiac septal defect syndrome" or filter by Orphanet code ORPHA:467176 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 hypotonia-psychomotor developmental delay-strabismus-cardiac septal defect syndrome trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Severe hypotonia-psychomotor developmental delay-strabismus-cardiac septal defect syndrome. Updated daily.