Journal article
Authors list: Neubauer, Bernd A.; Hahn, Andreas
Publication year: 2014
Pages: S89-S95
Journal: Epileptic Disorders
Volume number: 16
ISSN: 1294-9361
eISSN: 1950-6945
DOI Link: https://doi.org/10.1684/epd.2014.0688
Publisher: Wiley
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 style: Neubauer, 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 style: Neubauer, 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 MUTATIONS; ENCEPHALOPATHY; EPILEPSIA-PARTIALIS-CONTINUA; ETIOLOGY; MIGRATING PARTIAL SEIZURES; OHTAHARA SYNDROME; PREDICTORS; prolonged seizures; RECURRENCE; STATUS EPILEPTICUS