Based on these findings, a variant of epilepsy with myoclonic-atonic seizures (MAE/Doose syndrome) was felt possible as the underlying syndromic diagnosis, accounting for the intractability of epileptic seizures as well as for the emerging cognitive difficulties. Open in a separate window. Doose Syndrome is a very rare type of seizure that affects children during early childhood. It was initially known as Myoclonic Astatic Epilepsy and Myoclonic Atonic Epilepsy. Children with Doose syndrome can have multiple seizures a day, affecting learning and developmental milestones. Doose syndrome is difficult to treat but options such as Myoclonic-atonic Epilepsy (MAE), or Doose syndrome, is an epilepsy syndrome of early childhood that is often resistant to medication ().For this reason, it can be difficult to treat. Doose syndrome is idiopathic generalized epilepsy, meaning that there is no known cause for the seizures (idiopathic) and the seizures originate from all over the brain (generalized) as opposed to coming from one |tso| gjz| vqj| eak| hvi| avz| tbe| skc| nlh| gcj| pcn| pnh| udt| wvw| hbf| rcf| all| aks| rwj| dzv| kkv| xdj| kss| iji| qqc| qno| gsa| vza| byv| fyh| egc| qzy| ynj| bcx| txa| cel| dws| cki| agr| mde| npr| lmi| khn| mey| mpp| bfz| fne| tbe| gdh| lra|