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Doose syndrome: Difference between revisions
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<ref>http://www.epilepsy.com/learn/types-epilepsy-syndromes/doose-syndrome</ref> | <ref>http://www.epilepsy.com/learn/types-epilepsy-syndromes/doose-syndrome</ref> | ||
[http://onlinelibrary.wiley.com/doi/10.1111/j.1469-8749.2010.03744.x/epdf ] | [http://onlinelibrary.wiley.com/doi/10.1111/j.1469-8749.2010.03744.x/epdf Doose syndrome (myoclonic–astatic epilepsy): 40 years of progress] | ||
[http://onlinelibrary.wiley.com/doi/10.1111/j.1528-1167.2008.01765.x/full Optimal clinical management of children receiving the ketogenic diet: Recommendations of the International Ketogenic Diet Study Group] | [http://onlinelibrary.wiley.com/doi/10.1111/j.1528-1167.2008.01765.x/full Optimal clinical management of children receiving the ketogenic diet: Recommendations of the International Ketogenic Diet Study Group] | ||
<references/> | <references/> | ||
Revision as of 00:36, 22 August 2017
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]
Doose syndrome (myoclonic–astatic epilepsy): 40 years of progress