Disease Directory Parkinsonian-pyramidal syndrome
Neurological

Parkinsonian-pyramidal syndrome

Type

Disease

Gene

SNCA, FBXO7

About Parkinsonian-pyramidal syndrome

Parkinsonian-pyramidal syndrome is a rare disease catalogued by Orphanet (ORPHA:171695). It is associated with the SNCA, FBXO7 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 Parkinsonian-pyramidal syndrome trials.

Search ClinicalTrials.gov for "Parkinsonian-pyramidal syndrome" or filter by Orphanet code ORPHA:171695 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

Patient Organization

Orphanet

Visit website ↗

Orphanet

European reference resource for rare diseases (ORPHA:171695)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

Search NORD ↗

Find recruiting Parkinsonian-pyramidal syndrome trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for Parkinsonian-pyramidal syndrome. Updated daily.