About Intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome
Intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome is a rare disease catalogued by Orphanet (ORPHA:457279). It is associated with the PPP2R5D 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 Intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome trials.
Search ClinicalTrials.gov for "Intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome" or filter by Orphanet code ORPHA:457279 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 Intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Intellectual disability-macrocephaly-hypotonia-behavioral abnormalities syndrome. Updated daily.