ILAE Genetic Literacy Series: Self‐limited familial epilepsy syndromes with onset in neonatal age and infancy

The self‐limited (familial) epilepsies with onset in neonates or infants, formerly called benign familial neonatal and/or infantile epilepsies, are autosomal dominant disorders characterized by neonatal‐ or infantile‐onset focal motor seizures and the absence of neurodevelopmental complications. Sei...

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Veröffentlicht in:	Epileptic disorders 2023-08, Vol.25 (4), p.445-453
Hauptverfasser:	Millevert, Charissa, Weckhuysen, Sarah, Perucca, Piero, Cross, J. Helen, Lerche, Holger, Esterhuizen, Alina I., Lopes‐Cendes, Iscia, Tsai, Meng‐Han, Berkovic, Samuel F., Lowenstein, Daniel H., Tan, Nigel C. K., Helbig, Ingo, Mefford, Heather C., Brunklaus, Andreas, Lesca, Gaetan
Format:	Artikel
Sprache:	eng
Schlagworte:	Children Epilepsy Genetic counseling Genetic screening Infants KCNQ2 KCNQ3 Neonates PRRT2 SCN2A SCN8A Seizures self‐limited familial epilepsy
Online-Zugang:	Volltext
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