De novo late-onset absence status epilepticus or late-onset idiopathic generalized epilepsy? A case report and systematic review of the literature

2018 ◽  
Vol 20 (2) ◽  
pp. 123-131 ◽  
Author(s):  
Francesco Brigo ◽  
Veronica Tavernelli ◽  
Raffaele Nardone ◽  
Eugen Trinka
Seizure ◽  
2011 ◽  
Vol 20 (8) ◽  
pp. 655-658 ◽  
Author(s):  
Stefano Pro ◽  
Edoardo Vicenzini ◽  
Franco Randi ◽  
Patrizia Pulitano ◽  
Oriano Mecarelli

2012 ◽  
Vol 106 (4) ◽  
pp. 462-469 ◽  
Author(s):  
Lisa D. Hobson-Webb ◽  
Alan D. Proia ◽  
Beth L. Thurberg ◽  
Suhrad Banugaria ◽  
Sean N. Prater ◽  
...  

2020 ◽  
Vol 63 (4) ◽  
pp. 103825
Author(s):  
Keishiro Kinoshita ◽  
Yoshito Ishizaki ◽  
Hiroyuki Yamamoto ◽  
Motoshi Sonoda ◽  
Kousuke Yonemoto ◽  
...  

2016 ◽  
Vol 2016 ◽  
pp. 1-4
Author(s):  
Scott J. Adams ◽  
Melody Wong ◽  
Tahereh Haji ◽  
Shahmir Sohail ◽  
Salah Almubarak

Absence status epilepticus is characterized by a prolonged state of impaired consciousness or altered sensorium with generalized electroencephalographic abnormalities. It is most commonly diagnosed in patients with known idiopathic generalized epilepsy; however, it may also be the first presentation of epilepsy. Due to the subtle and variable manifestations of the condition, absence status epilepticus may be underrecognized, particularly in children. We present the case of an 8-year-old boy who experienced two episodes of prolonged altered mental status, subsequently determined to be absence status epilepticus with idiopathic generalized epilepsy with phantom absences. We discuss the classification, pathophysiology, clinical presentation, and electroencephalographic findings of pediatric absence status epilepticus and provide a practical overview for management.


2018 ◽  
Vol 138 (3) ◽  
pp. 259-262 ◽  
Author(s):  
P. S. Reif ◽  
A. Männer ◽  
L. M. Willems ◽  
L. Kay ◽  
J. P. Zöllner ◽  
...  

2014 ◽  
Vol 2014 ◽  
pp. 1-8 ◽  
Author(s):  
Leonilda Bilo ◽  
Sabina Pappatà ◽  
Roberto De Simone ◽  
Roberta Meo

The authors review the literature for cases fulfilling the criteria for the proposed idiopathic generalized epilepsy syndrome (IGE) of absence status epilepsy described by Genton et al. (2008). Difficulties arising in diagnosing such cases are remarked, and possible overlapping with other proposed IGE syndromes is discussed.


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