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Any rolandic epilepsy-speech dyspraxia syndrome in which the cause of the disease is a variation in GRIN2A gene.
No clinical trials have been registered for GRIN2A-related rolandic epilepsy-speech dyspraxia syndrome.
2 publications have been identified in PubMed for GRIN2A-related rolandic epilepsy-speech dyspraxia syndrome. Research spans Case Report / Case Series (50%) and Epidemiology / Natural History (50%).
Ebrahim AK (2025). [PMID: 40727434](https://pubmed.ncbi.nlm.nih.gov/40727434/). *Case reports in pediatrics*. [Case Report / Case Series]
Paprocka J (2024). [PMID: 38837855](https://pubmed.ncbi.nlm.nih.gov/38837855/). *Epilepsia open*. [Epidemiology / Natural History]
Data assembled from 2 of 12 sources · Last updated Sep 20, 2026, 4:38 PM UTC
Common questions about GRIN2A-related rolandic epilepsy-speech dyspraxia syndrome