Ketogenic diet to manage refractory epilepsy in the cdkl5 disorder
Objectives: Mutations involving the CDKL5 gene have been identified as a cause of severe epileptic encephalopathy, often later presenting with features similar to Rett syndrome.1 Cardinal features of epilepsy in the CDKL5 disorder include early onset at a median age of six weeks and poor response to...
| Main Authors: | , , , |
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| Format: | Conference Paper |
| Published: |
BMJ Publishing Group
2017
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| Online Access: | http://hdl.handle.net/20.500.11937/74467 |