Benign familial neonatal epilepsy (Q91658): Difference between revisions

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Latest revision as of 18:41, 15 August 2026

Epilepsy of the newborn characterised by frequent brief seizures within the first few days of life. Onset may be as late as 3 months of age. Seizures typically remit spontaneously within 6 weeks. The ictal electroencephalogram shows initial diffuse flattening followed by bilateral spikes and sharp waves. The cause is an autosomal dominant channelopathy with mutations in the voltage-gated potassium channel genes KCNQ2 or KCNQ3.

Language	Label	Description	Also known as
default for all languages	ID_1948859880
English	Benign familial neonatal epilepsy	Epilepsy of the newborn characterised by frequent brief seizures within the first few days of life. Onset may be as late as 3 months of age. Seizures typically remit spontaneously within 6 weeks. The ictal electroencephalogram shows initial diffuse flattening followed by bilateral spikes and sharp waves. The cause is an autosomal dominant channelopathy with mutations in the voltage-gated potassium channel genes KCNQ2 or KCNQ3.