Severe myoclonic epilepsy of infancy
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(Redirected from Dravet syndrome)
Severe myoclonic epilepsy of infancy also known as Dravet syndrome is a type of epilepsy with seizures that are often triggered by hot temperatures or fever. It often begins around six months of age.
- Lhatoo, edited by Simon Shorvon, Renzo Guerrini, Mark Cook, Samden D. (2013). Oxford textbook of epilepsy and epileptic seizures. Oxford [u.a.]: Oxford Univ. Press. p. 13. ISBN 9780199659043.