Dravet syndrome: diverse seizure phenotypes with various triggers and developmental outcome- A case series from a LMIC.

Abstract excerpt

Dravet syndrome (DS) is a severe childhood epilepsy characterised by drug-resistant seizures, developmental delays, and behavioural disturbances, often linked to de novo mutations in the SCN1A gene. This retrospective case series from Aga Khan University Hospital, Karachi, describes five patients with varying ages of seizure onset and difficult-to-control seizures despite conventional antiseizure medications....

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