Benign familial neonatal epilepsy (Q91658): Difference between revisions

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Epilepsia do recém-nascido caracterizada por convulsões frequentes e curtas nos primeiros dias de vida. Início pode ocorrer até os 3 meses de idade. As convulsões tipicamente remitem espontaneamente em 6 semanas. O eletroencefalograma ictal mostra achatamento difuso inicial seguido por picos bilaterais e ondas agudas. A causa é uma canalopatia autossômica dominante com mutações nos genes de canal de potássio voltagem-dependente KCNQ2 ou KCNQ3.
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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.

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.
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    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.

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