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Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12710/11011
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dc.contributor.authorSatula, Victoria-
dc.date.accessioned2020-07-06T17:03:45Z-
dc.date.available2020-07-06T17:03:45Z-
dc.date.issued2018-
dc.identifier.citationSATULA, Victoria. Epileptic encephalopathy: Doose syndrome. In: MedEspera: the 7th Internat. Medical Congress for Students and Young Doctors: abstract book. Chișinău: S. n., 2018, p. 52-53.en_US
dc.identifier.urihttps://medespera.asr.md/wp-content/uploads/Abastract-Book-2018.pdf-
dc.identifier.urihttp://repository.usmf.md/handle/20.500.12710/11011-
dc.descriptionNicolae Testemitanu State University of Medicine and Pharmacy of the Republic of Moldovaen_US
dc.description.abstractIntroduction. The term epileptic encephalopathies are severe brain disorders of early age with a different manifestation, depending on the age of onset, developmental outcome, etiologies, neuropsychological deficits, electroencephalographic (EEG) patterns, seizure types, and prognosis, but all may have a significant impact on neurological development. Doose syndrome, otherwise traditionally known as myoclonic-astatic epilepsy is an epileptic encephalopathy with multiple seizure types. About a third of children may have episodes of convulsive status epilepticus. The disease is characterized by the following criteria: genetic predisposition (high incidence of seizures and/or genetic EEG patterns in relatives); mostly normal development and no neurological deficits before onset; primarily generalized myoclonic, astatic or myoclonicastatic seizures, short absences and mostly generalized tonic-clonic seizures; no tonic seizures or tonic drop attacks during daytime, generalized EEG patterns, and often normal neuroimaging . The prognosis is variable and difficult to predict, and the seizures may remit in 54-89% of patients.en_US
dc.language.isoenen_US
dc.publisherMedEsperaen_US
dc.subjectepileptic encephalopathyen_US
dc.subjectDoose syndromeen_US
dc.subjectseizureen_US
dc.subjectelectroencephalographic (EEG) patternsen_US
dc.subjectGEFS+en_US
dc.titleEpileptic encephalopathy: Doose syndromeen_US
dc.typeArticleen_US
Appears in Collections:MedEspera 2018

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