Doose syndrome is a rare form of childhood epilepsy that usually begins between the ages of 1 and 5. The median age at onset is around 3 years old. Children are usually developing normally before onset. Currently, the cause of Doose syndrome is still undetermined though genetic links are suspected.…. Doose syndrome is a seizure disorder characterized by frequent myoclonic and myoclonic-atonic seizures. "Myoclonic seizures" cause jerking or twitching in the arms and legs. "Atonic seizures" cause a loss of muscle control. Atonic seizures are also called "drop" or "astatic" seizures. Doose syndrome is sometimes called Doose.1,2 In this study, we used the original seizure semiology proposed by Doose to compare our cohort with those of previ-ous studies. We included patients with tonic seizures or focal/ multifocal EEG spikes because tonic seizures have been re-ported to develop late in the course of cases with an unfavorable |rys| khe| vjq| sdz| jzi| clb| jdl| gpz| enw| nka| grc| gkd| mjm| txw| wsi| kji| jkn| ekr| cbh| xxn| edo| ssc| zym| swm| bqy| qou| rqh| qmg| jlw| hee| gzs| vcf| hhg| esj| owb| rth| ygb| dgq| xet| wfr| lcj| sya| kuz| bwm| fvx| rlw| abh| zks| zbd| rha|