Intravenous lacosamide for treatment of absence status epilepticus in genetic generalized epilepsy: A case report and review of literature

2018 ◽  
Vol 138 (3) ◽  
pp. 259-262 ◽  
Author(s):  
P. S. Reif ◽  
A. Männer ◽  
L. M. Willems ◽  
L. Kay ◽  
J. P. Zöllner ◽  
...  
Seizure ◽  
2011 ◽  
Vol 20 (8) ◽  
pp. 655-658 ◽  
Author(s):  
Stefano Pro ◽  
Edoardo Vicenzini ◽  
Franco Randi ◽  
Patrizia Pulitano ◽  
Oriano Mecarelli

2019 ◽  
Vol 10 ◽  
Author(s):  
Lorenza Di Genova ◽  
Katia Perruccio ◽  
Maria Grazia Celani ◽  
Elena Mastrodicasa ◽  
Teresa Anna Cantisani ◽  
...  

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.


2006 ◽  
Vol 3 (1) ◽  
pp. 55-57 ◽  
Author(s):  
S Dwarakanath ◽  
S Gopal ◽  
R Satish ◽  
NK Venkataramana

2009 ◽  
Author(s):  
S.R.K. Naik ◽  
S. Kang ◽  
Ch. Ling ◽  
Regina

Author(s):  
Anes Mašović ◽  
Ibrahim Omerhodžić ◽  
Emina Hrvat ◽  
Lejla Gurbeta ◽  
Edin Begić ◽  
...  

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