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Doose syndrome: Difference between revisions
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[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] | ||
==ILAE== | == [[International_League_Against_Epilepsy| ILAE]]== | ||
Version [[1989]] | Version [[1989]] | ||
[[epilepsy with mioclonic atonic seizures]] | [[epilepsy with mioclonic atonic seizures]] | ||
==Treatment== | ==Treatment== | ||
Latest revision as of 16:09, 21 March 2019
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
ILAE
Version 1989
epilepsy with mioclonic atonic seizures