About Kyphoscoliosis-lateral tongue atrophy-hereditary spastic paraplegia syndrome
Kyphoscoliosis-lateral tongue atrophy-hereditary spastic paraplegia syndrome is a rare disease catalogued by Orphanet (ORPHA:496689). It is associated with the KY 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 Kyphoscoliosis-lateral tongue atrophy-hereditary spastic paraplegia syndrome trials.
Search ClinicalTrials.gov for "Kyphoscoliosis-lateral tongue atrophy-hereditary spastic paraplegia syndrome" or filter by Orphanet code ORPHA:496689 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 Kyphoscoliosis-lateral tongue atrophy-hereditary spastic paraplegia syndrome trials
Search 500,000+ studies from ClinicalTrials.gov, filtered for Kyphoscoliosis-lateral tongue atrophy-hereditary spastic paraplegia syndrome. Updated daily.