Literature DB >> 29325826

Myoclonic absence seizures with complex gestural automatisms.

Kenneth A Myers1, Ingrid E Scheffer2.   

Abstract

Epilepsy with myoclonic absences is a rare generalized epilepsy syndrome with distinctive seizures. Two unrelated children had mild developmental impairment and onset of myoclonic-absences at 3 and 8 years. Seizures were characterized by bilateral 3 Hz myoclonic jerks superimposed on tonic abduction of the upper limbs. Events lasted 10-60 s, and complex gestural automatisms were often observed; in one case, a boy undid his seatbelt and attempted to exit a moving vehicle. Post-ictally, both children immediately regained awareness without recollection of their actions. Ictal EEGs showed 3 Hz generalized spike-wave. Complex automatisms have not been described in myoclonic absence seizures. This generalized seizure type can be confused with focal seizures when these ictal behaviours occur.
Copyright © 2017 European Paediatric Neurology Society. Published by Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  Automatisms; Genetic generalized epilepsy; Myoclonic absence epilepsy; Myoclonic absence seizures

Mesh:

Year:  2017        PMID: 29325826     DOI: 10.1016/j.ejpn.2017.12.003

Source DB:  PubMed          Journal:  Eur J Paediatr Neurol        ISSN: 1090-3798            Impact factor:   3.140


  1 in total

1.  Seizures in Sotos syndrome: Phenotyping in 49 patients.

Authors:  Olivier Fortin; Christian Vincelette; Afsheen Q Khan; Saoussen Berrahmoune; Christelle Dassi; Mitra Karimi; Ingrid E Scheffer; Jun Lu; Kellie Davis; Kenneth A Myers
Journal:  Epilepsia Open       Date:  2021-04-09
  1 in total

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