About Neurogenic scapuloperoneal syndrome, Kaeser type
Neurogenic scapuloperoneal syndrome, Kaeser type is a rare disease catalogued by Orphanet (ORPHA:85146). It is associated with the DES 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 Neurogenic scapuloperoneal syndrome, Kaeser type trials.
Search ClinicalTrials.gov for "Neurogenic scapuloperoneal syndrome, Kaeser type" or filter by Orphanet code ORPHA:85146 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 Neurogenic scapuloperoneal syndrome, Kaeser type trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Neurogenic scapuloperoneal syndrome, Kaeser type. Updated daily.