Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/13642
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dc.contributor.authorSingh, Ren
dc.contributor.authorScheffer, Ingrid Een
dc.contributor.authorCrossland, Ken
dc.contributor.authorBerkovic, Samuel Fen
dc.date.accessioned2015-05-16T03:31:19Z
dc.date.available2015-05-16T03:31:19Z
dc.date.issued1999-01-01en
dc.identifier.citationAnnals of Neurology; 45(1): 75-81en
dc.identifier.govdoc9894880en
dc.identifier.otherPUBMEDen
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/13642en
dc.description.abstractWe examined the phenotypic variation and clinical genetics in nine families with generalized epilepsy with febrile seizures plus (GEFS+). This genetic epilepsy syndrome with heterogeneous phenotypes was hitherto described in only one family. We obtained genealogical information on 799 individuals and conducted detailed evaluation of 272 individuals. Ninety-one individuals had a history of seizures and 63 had epilepsy consistent with the GEFS+ syndrome. Epilepsy phenotypes were febrile seizures (FS) in 31, febrile seizures plus (FS+) in 15, FS+ with other seizure types (atonic, myoclonic, absence, or complex partial) in 8, and myoclonic-astatic epilepsy in 9 individuals. Inheritance was autosomal dominant with approximately 60% penetrance. This study confirms and expands the spectrum of GEFS+ and provides new insights into the phenotypic relationships and genetics of FS and the generalized epilepsies of childhood. Moreover, the ability to identify large families with this newly recognized common, childhood-onset, generalized genetic epilepsy syndrome suggests that it should be a prime target for attempts to identify genes relevant to FS and generalized epilepsy.en
dc.language.isoenen
dc.subject.otherAdulten
dc.subject.otherAge of Onseten
dc.subject.otherElectroencephalographyen
dc.subject.otherEpilepsies, Myoclonic.diagnosis.geneticsen
dc.subject.otherEpilepsy, Absence.diagnosis.geneticsen
dc.subject.otherEpilepsy, Generalized.classification.diagnosis.geneticsen
dc.subject.otherFamily Healthen
dc.subject.otherFemaleen
dc.subject.otherHumansen
dc.subject.otherInfanten
dc.subject.otherMaleen
dc.subject.otherPedigreeen
dc.subject.otherPhenotypeen
dc.subject.otherSeizures, Febrile.diagnosis.geneticsen
dc.titleGeneralized epilepsy with febrile seizures plus: a common childhood-onset genetic epilepsy syndrome.en
dc.typeJournal Articleen
dc.identifier.journaltitleAnnals of Neurologyen
dc.identifier.affiliationDepartment of Medicine (Neurology), University of Melbourne, Austin and Repatriation Medical Center, Victoria, Australiaen
dc.description.pages75-81en
dc.relation.urlhttps://pubmed.ncbi.nlm.nih.gov/9894880en
dc.type.austinJournal Articleen
local.name.researcherBerkovic, Samuel F
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-
crisitem.author.deptEpilepsy Research Centre-
crisitem.author.deptNeurology-
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