Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/17328
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dc.contributor.authorMyers, Kenneth A-
dc.contributor.authorScheffer, Ingrid E-
dc.date2017-12-19-
dc.date.accessioned2018-04-03T04:55:59Z-
dc.date.available2018-04-03T04:55:59Z-
dc.date.issued2018-05-
dc.identifier.citationEuropean journal of paediatric neurology : EJPN 2018; 22(3): 532-535-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/17328-
dc.description.abstractEpilepsy 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.-
dc.language.isoeng-
dc.subjectAutomatisms-
dc.subjectGenetic generalized epilepsy-
dc.subjectMyoclonic absence epilepsy-
dc.subjectMyoclonic absence seizures-
dc.titleMyoclonic absence seizures with complex gestural automatisms.-
dc.typeJournal Article-
dc.identifier.journaltitleEuropean journal of paediatric neurology : EJPN-
dc.identifier.affiliationEpilepsy Research Centre, Department of Medicine, Austin Health, The University of Melbourne, Heidelberg, Victoria, Australia-
dc.identifier.affiliationDepartment of Paediatrics, The University of Melbourne, Parkville, Victoria, Australia-
dc.identifier.affiliationThe Florey Institute of Neuroscience and Mental Health, Heidelberg, Victoria, Australia-
dc.identifier.affiliationDepartment of Neurology, Royal Children's Hospital, Parkville, Victoria, Australia-
dc.identifier.doi10.1016/j.ejpn.2017.12.003-
dc.identifier.orcid0000-0002-2311-2174-
dc.identifier.orcid0000-0001-7831-4593-
dc.identifier.pubmedid29325826-
dc.type.austinJournal Article-
local.name.researcherScheffer, Ingrid E
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
item.openairetypeJournal Article-
item.grantfulltextnone-
item.languageiso639-1en-
crisitem.author.deptEpilepsy Research Centre-
Appears in Collections:Journal articles
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