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KCNQ2 Neonatal Epilepsy

Prevalence: 1/100000

neurological

Official·OMIM:121200 Official·ORPHA1949

Benign familial neonatal seizures due to KCNQ2 gene mutations.

Associated Genes

KCNQ2Potassium Voltage-Gated Channel Subfamily Q Member 2

Chromosome 20Autosomal Dominant