Journal article

Syndromes at risk of status epilepticus in children: genetic and pathophysiological issues


Authors listNeubauer, Bernd A.; Hahn, Andreas

Publication year2014

PagesS89-S95

JournalEpileptic Disorders

Volume number16

ISSN1294-9361

eISSN1950-6945

DOI Linkhttps://doi.org/10.1684/epd.2014.0688

PublisherWiley


Abstract
Status epilepticus (SE) is a medical emergency with increased risk of morbidity and mortality in all age groups. Recent research has identified a variety of new genes implicated in disorders with severe epilepsies as a prominent feature. Autoimmune mechanisms have also been recently recognised as a cause of epilepsies with SE as a characteristic symptom. Knowledge about the aetiology potentially underlying SE may help to guide diagnostics and eventually influence treatment decisions. This review recapitulates, in brief, the risk of SE in specific clinical settings, provides an overview of paediatric epilepsy syndromes more commonly, or by definition, associated with SE, and summarizes some recent research data on genetic defects and disease mechanisms implicated in the pathogenesis of epilepsies frequently accompanied by SE.



Citation Styles

Harvard Citation styleNeubauer, B. and Hahn, A. (2014) Syndromes at risk of status epilepticus in children: genetic and pathophysiological issues, Epileptic Disorders, 16, pp. S89-S95. https://doi.org/10.1684/epd.2014.0688

APA Citation styleNeubauer, B., & Hahn, A. (2014). Syndromes at risk of status epilepticus in children: genetic and pathophysiological issues. Epileptic Disorders. 16, S89-S95. https://doi.org/10.1684/epd.2014.0688



Keywords


DE-NOVO MUTATIONSENCEPHALOPATHYEPILEPSIA-PARTIALIS-CONTINUAETIOLOGYMIGRATING PARTIAL SEIZURESOHTAHARA SYNDROMEPREDICTORSprolonged seizuresRECURRENCESTATUS EPILEPTICUS

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