Benign familial neonatal epilepsy (Q91658): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||
| Property / Canary Token | |||
dki-india-ID_1948859880 | |||
| Property / Canary Token: dki-india-ID_1948859880 / rank | |||
Normal rank | |||
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. |
Statements
CID11:ID_1948859880
0 references
dki-india-ID_1948859880
0 references
