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Extending the KCNQ2 encephalopathy Spectrum Neurol 81:1697-1703, Weckhuysen, S.,et al, 2013 See this aricle in Pubmed Article Abstract KCNQ2 mutations cause approximately 13% of unexplained NEE. Patients present with a wide spectrum of severity and, although rare, infantile epilepsy onset is possible.

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(click to filter results - removes previous filter) burst suppression pattern,electroencephalogram children electroencephalogram,abnormalities of encephalopathy encephalopathy,neonatal familial gene mutation KCNQ2 encephalopathy MRI,abnormal screening seizure seizure,drug resistance seizure,neonatal

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