About Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly
Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly is a rare disease catalogued by Orphanet (ORPHA:402364). It is associated with the MED17 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 Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly trials.
Search ClinicalTrials.gov for "Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly" or filter by Orphanet code ORPHA:402364 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 Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly. Updated daily.