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rolandic epilepsy-speech dyspraxia syndrome - Clinical Profile, Genes & Research | Kisho | Kisho

Rare Disease

rolandic epilepsy-speech dyspraxia syndrome

MONDO:0015587

Overview

A rare, genetic epilepsy characterized by speech disorder (including a range of symptoms from dysarthria, speech dyspraxia, receptive and expressive language delay/regression and acquired aphasia to subtle impairments of conversational speech) and epilepsy (mostly focal and secondary generalized childhood-onset seizures, sometimes with aura). Mild to severe intellectual disability may also be observed.

ResearchLimited published research (3 articles)

Prognosis

Estimated prevalence: Unknown (Unknown prevalence).

Research Landscape

Sourced from ClinicalTrials.gov and PubMed. Publication types are classified using NLM-curated article metadata; research type breakdowns reflect the nature of published work for this disease.

No clinical trials have been registered for rolandic epilepsy-speech dyspraxia syndrome.

3 publications have been identified in PubMed for rolandic epilepsy-speech dyspraxia syndrome. Research spans Case Report / Case Series (67%) and Basic Science / Preclinical (33%).

Recent Publications

Coburn RP (2026). [PMID: 41996995](https://pubmed.ncbi.nlm.nih.gov/41996995/). *Cortex*. [Case Report / Case Series]
Bertagnoli S (2025). [PMID: 40973146](https://pubmed.ncbi.nlm.nih.gov/40973146/). *Arch Clin Neuropsychol*. [Case Report / Case Series]
Anastasopoulou I (2025). [PMID: 40180575](https://pubmed.ncbi.nlm.nih.gov/40180575/). *J Neurosci*. [Basic Science / Preclinical]

Data assembled from 3 of 12 sources · Last updated Sep 19, 2026, 3:34 AM UTC

MONDOHPOClinicalTrials.govFDAPubMedHGNCClinVarClinGenGeneReviewsOrphanetOMIMRUSP

Medical References

External Resources

Orphanet

European rare disease database

Orphanet:163721

GARD

Genetic and Rare Diseases Info Center

GARD:17002

Questions for Your Care Team

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rolandic epilepsy-speech dyspraxia syndrome

Overview

Prognosis

Research Landscape

Recent Publications

Medical References

External Resources

Orphanet

GARD

Subtypes

Related Diseases

Questions for Your Care Team

Questions for Your Care Team