Disease Directory Rolandic epilepsy-speech dyspraxia syndrome
Neurological

Rolandic epilepsy-speech dyspraxia syndrome

Type

Disease

Gene

SRPX2, GRIN2A

About Rolandic epilepsy-speech dyspraxia syndrome

Rolandic epilepsy-speech dyspraxia syndrome is a rare disease catalogued by Orphanet (ORPHA:163721). It is associated with the SRPX2, GRIN2A 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 Rolandic epilepsy-speech dyspraxia syndrome trials.

Search ClinicalTrials.gov for "Rolandic epilepsy-speech dyspraxia syndrome" or filter by Orphanet code ORPHA:163721 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:163721)

View on Orphanet ↗

NORD

National Organization for Rare Disorders

Search NORD ↗

Find recruiting Rolandic epilepsy-speech dyspraxia syndrome trials

Search 500,000+ studies from ClinicalTrials.gov, filtered for Rolandic epilepsy-speech dyspraxia syndrome. Updated daily.