Should we still consider Dravet syndrome an epileptic encephalopathy?

Epilepsy Behav. 2014 Jul:36:80-1. doi: 10.1016/j.yebeh.2014.05.010. Epub 2014 Jun 2.

Author

Stéphane Auvin¹

Affiliation

¹ INSERM U1141, 75019 Paris, France; APHP, Hôpital Robert Debré, Service de Neurologie Pédiatrique, 75019 Paris, France; Univ Paris Diderot, Sorbonne Paris Cité, INSERM UMR1141, 75019 Paris, France. Electronic address: stephane.auvin@inserm.fr.

PMID: 24892752
DOI: 10.1016/j.yebeh.2014.05.010

No abstract available

Publication types

Editorial

MeSH terms

Epilepsies, Myoclonic / diagnosis*
Epilepsies, Myoclonic / genetics
Humans
Infant
NAV1.1 Voltage-Gated Sodium Channel / genetics
Spasms, Infantile / genetics
Spasms, Infantile / physiopathology*

Substances

NAV1.1 Voltage-Gated Sodium Channel