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Article

The first Korean case of KCNQ2 mutation in a family with benign familial neonatal convulsions.

Journal of Korean medical science - 1 Feb 2010

Yum Mi-Sun, Ko Tae-Sung, Yoo Han-Wook

Abstract excerpt

Neonatal seizures represent a heterogeneous group of disorders with vastly different etiologies and outcomes. Benign familial neonatal convulsions (BFNC) are a distinctive epileptic syndrome of autosomal dominant inheritance with a favorable prognosis, characterized by the occurrence of unprovoked partial or generalized clonic seizures in the neonatal period or early infancy. Recently, mutations in two potassium...

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Share to Electroencephalography
Share to Epilepsy, Benign Neonatal
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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to KCNQ2 Potassium Channel

Share to Magnetic Resonance Imaging

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Source

Open in PubMed Open full text

Identifiers

PMID: 20119593
DOI: 10.3346/jkms.2010.25.2.324
PMCID: PMC2811307

Genes

KCNQ2
KCNQ3

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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The first Korean case of KCNQ2 mutation in a family with benign familial neonatal convulsions.PMID 20119593Read ↗

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[A novel mutation in KCNQ2 gene causes benign familial infantile convulsions (BFIC) in a Chinese family].Semantic proximity Read ↗

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A de novo KCNQ2 mutation detected in non-familial benign neonatal convulsions.Semantic proximity Read ↗

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