About this Research Topic
The aim of this Research Topic is to further elucidate the basis of early childhood epilepsies. This will allow more precise investigation and classification of clinical syndromes, as well as the underlying etiology in children that meet criteria for an epileptic syndrome, and those in whom syndromic classification is not possible. We also aim to inform readers of efficiencies that can be made within investigation in terms of either technological development (e.g genomic techniques), as well as appropriate targeting. This could then lead to the correlation of accurate classification with appropriate therapy, and specifically the identification of more precise therapies. This could greatly benefit groups such as children affected by clinical syndromes (e.g. Ohtahara), as well as those with specific results on investigation (e.g. Lissencephaly) or variants in a novel or known gene such as STXBP1.
This Research Topic welcomes submissions of innovative reports which would enlighten the reader on the causation, investigation and management of early onset epilepsies, including innovative literature reviews, and controlled trials. The manuscripts may focus on both rarer epilepsy syndromes, as well as wider classification groups such as the genetic or focal epilepsies. We especially welcome submissions on the following:
• Genomic analysis of early onset epilepsies;
• MRI and its uses in the diagnosis of early onset epilepsies;
• Inborn errors of metabolism and their biochemical investigation;
• The evidence base for modern therapies for early onset epilepsies;
• Targeted “precise” treatments.
We would like to acknowledge that Dr. Sam Amin, University of Bristol, has acted as a coordinator and has contributed to the preparation of the proposal for this Research Topic.
Keywords: Epilepsy, Encephalopathy, Genomic, Child, Infant
Important Note: All contributions to this Research Topic must be within the scope of the section and journal to which they are submitted, as defined in their mission statements. Frontiers reserves the right to guide an out-of-scope manuscript to a more suitable section or journal at any stage of peer review.