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Doose syndrome

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Myoclonic astatic epilepsy was first described by Hermann Doose in 1970. It is an uncommon epilepsy that account 1-2% of all childhood epilepsies[1]

Links

Doose syndrome (myoclonic–astatic epilepsy): 40 years of progress

Optimal clinical management of children receiving the ketogenic diet: Recommendations of the International Ketogenic Diet Study Group

ILAE

Version 1989

epilepsy with mioclonic atonic seizures

Treatment

ketogenic diet

  1. ↑ http://www.epilepsy.com/learn/types-epilepsy-syndromes/doose-syndrome
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