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Dravet syndrome is often a developmental and epileptic encephalopathy which has early onset and is particularly characterised by reoccurring fever linked extended hemiclonic seizures with afebrile generalised tonic clinic seizures, myoclonic seizures and absence seizures. Eventually, small children with Dravet syndrome produce critical learning disabilities, impaired language and feeding issues. Provided the issues in managing Dravet syndrome, the choice of seizures it might function, as well as effects it can have on quality of life both equally for children with Dravet syndrome and their carers, the committee agreed to propose that people with Dravet syndrome must have an Grownup or paediatric neurologist with expertise in epilepsy linked to their care Using the purpose of facilitating diagnosis, increasing entry to even more investigations, and making certain that correct remedy is presented.

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Currently, Dravet Syndrome stays Probably the most treatment resistant prescription drugs and fantastic seizure Management is rare, with not many kids/Grown ups living seizure-free of charge.

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Financial proof analysis for assessment problem: What antiseizure therapies (monotherapy or include-on) are powerful during pokienet the therapy of seizures in Dravet syndrome?

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