KCNQ2 Encephalopathy Showing a Distinct Ictal Amplitude-Integrated Electroencephalographic Pattern
KCNQ2 mutations induce a neonatal-onset epileptic encephalopathy of widely varying severity, ranging from benign familial neonatal epilepsy to severe refractory epileptic encephalopathy. Refractory seizures with KCNQ2 mutations have a positive response to sodium-channel blockers. Recently, a distinc...
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| Main Authors: | , , , , , |
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| Format: | Book |
| Published: |
Korean Society of Neonatology,
2020-11-01T00:00:00Z.
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| Online Access: | Connect to this object online. |
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