Disease Directory Periodic paralysis with later-onset distal motor neuropathy
Rare Disease

Periodic paralysis with later-onset distal motor neuropathy

Type

Disease

Gene

MT-ATP6, MT-ATP8

About Periodic paralysis with later-onset distal motor neuropathy

Periodic paralysis with later-onset distal motor neuropathy is a rare disease catalogued by Orphanet (ORPHA:397750). It is associated with the MT-ATP6, MT-ATP8 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 Periodic paralysis with later-onset distal motor neuropathy trials.

Search ClinicalTrials.gov for "Periodic paralysis with later-onset distal motor neuropathy" or filter by Orphanet code ORPHA:397750 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:397750)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

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Find recruiting Periodic paralysis with later-onset distal motor neuropathy trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for Periodic paralysis with later-onset distal motor neuropathy. Updated daily.