Not all SCN1A epileptic encephalopathies are Dravet syndrome
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DOI: 10.1212/wnl.0000000000004331
Abstract: Objective: To define a distinct SCN1A developmental and epileptic encephalopathy with early onset, profound impairment, and movement disorder. Methods: A case series of 9 children were identified with a profound developmental and epileptic encephalopathy and… read more here.
Keywords: profound developmental; movement disorder; dravet syndrome; scn1a ... See more keywords