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Doose syndrome: Difference between revisions
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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 | Myoclonic astatic [[epilepsy]] was first described by [[Hermann Doose]] in 1970. It is an uncommon epilepsy that account 1-2% of all childhood epilepsies<ref>http://www.epilepsy.com/learn/types-epilepsy-syndromes/doose-syndrome</ref> | ||
<ref>http://www.epilepsy.com/learn/types-epilepsy-syndromes/doose-syndrome</ref><references/> | ==Links== | ||
[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] | |||
== [[International_League_Against_Epilepsy| ILAE]]== | |||
Version [[1989]] | |||
[[epilepsy with mioclonic atonic seizures]] | |||
==Treatment== | |||
[[ketogenic diet]] | |||
<references/> | |||
[[Category:Disease]] | |||
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