SCN2A encephalopathy A major cause of epilepsy of infancy with migrating focal seizures.


Twelve patients with an SCN2A epileptic encephalopathy underwent electroclinical phenotyping.


De novo SCN2A mutations have recently been associated with severe infantile-onset epilepsies. Herein, we define the phenotypic spectrum of SCN2A encephalopathy.


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Neurology (2015): 10-1212.
Howell, Katherine B. et al.