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March 6, 2011. Doose syndrome, which is also named as myoclonic-astatic epilepsy(MAE), is a rare epilepsy syndrome of children. 94% patients onset before age of 5, with a peak of 3-4 year-old. Usually, they are normal children before onset. There are special Electroencephalogram(EEG) findings in Doose patients. Considering the complexity of EEG, I will skip this part to avoid giving you confusion. Doose syndrome needs to be differentiated from Dravet syndrome, West syndrome, febrile convulsion, Lennox-Ga...

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