Articles with "kcnq2 gene" as a keyword



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A de novo KCNQ2 Gene Mutation Associated With Non-familial Early Onset Seizures: Case Report and Revision of Literature Data

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Published in 2019 at "Frontiers in Pediatrics"

DOI: 10.3389/fped.2019.00348

Abstract: Among neonatal epileptic syndromes, benign familial neonatal seizures (BFNS) are often due to autosomal-dominant mutations of the KCNQ2 gene. Seizures are usually characterized by asymmetric tonic posturing with apnea with onset in the first 7… read more here.

Keywords: novo kcnq2; case; kcnq2 gene; tonic seizures ... See more keywords