Dravet syndrome an unusual cause of atypical febrile seizure: a case report

Dravet syndrome is a rare refractory epileptic encephalopathy with an underlying genetic basis. It presents with recurrent febrile seizures in infancy. Though development is normal in infancy, neurodevelopmental delay and neurologic disability begin after the onset of seizure at the age of around 2-4 years. The outcome can be improved by early diagnosis (genetic testing for SCN1A gene) and timely treatment. In this case report we are presenting a 3-year-old female child with recurrent refractory epilepsy associated with fever and was diagnosed with Dravet syndrome.