Clinical and genetic characteristics of patients with Doose syndrome

Abstract

MAE patients had genetic heterogeneity, and <i>HNRNPU</i> and <i>STS</i> emerged as possible candidate causative genes. Febrile seizures prior to epileptic seizures and myoclonic-atonic seizure at onset indicate a genetic predisposition to MAE. Comorbid conditions were not related to genetic predisposition to MAE.