Disease Directory Infantile-onset ascending hereditary spastic paralysis
Rare Disease

Infantile-onset ascending hereditary spastic paralysis

Type

Disease

Gene

ALS2

About Infantile-onset ascending hereditary spastic paralysis

Infantile-onset ascending hereditary spastic paralysis is a rare disease catalogued by Orphanet (ORPHA:293168). It is associated with the ALS2 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-onset ascending hereditary spastic paralysis trials.

Search ClinicalTrials.gov for "Infantile-onset ascending hereditary spastic paralysis" or filter by Orphanet code ORPHA:293168 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

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Orphanet

European reference resource for rare diseases (ORPHA:293168)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

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Find recruiting Infantile-onset ascending hereditary spastic paralysis trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for Infantile-onset ascending hereditary spastic paralysis. Updated daily.