Juvenile Absence Epilepsy

2012 ◽  
Keyword(s):  
Absence Epilepsy ◽  
Juvenile Absence Epilepsy

Juvenile Absence Epilepsy Exacerbated by Valproic Acid

2007 ◽  
Vol 36 (2) ◽  
pp. 121-124 ◽  
Author(s):  
Robbie D. Buechler ◽  
Jeffrey R. Buchhalter
Keyword(s):  
Valproic Acid ◽  
Absence Epilepsy ◽  
Juvenile Absence Epilepsy

Genetic generalized epilepsy

2016 ◽  
Author(s):  
Friederike Moeller ◽  
Ronit M. Pressler ◽  
J. Helen Cross
Keyword(s):  
Clinical Presentation ◽  
Age Of Onset ◽  
Juvenile Myoclonic Epilepsy ◽  
Absence Epilepsy ◽  
Childhood Absence Epilepsy ◽  
Juvenile Absence Epilepsy ◽  
Generalized Epilepsy ◽  
Treatment Prognosis ◽  
Electroencephalogram Eeg ◽  
Eeg Features

This chapter provides an overview of generalized epilepsies (GGE), which comprises a group of epilepsy syndromes of presumed genetic origin. They are classified into several syndromes according to their age, depending on clinical manifestation and associated electroencephalogram (EEG) features. The chapter introduces the concept of GGE before addressing different GGE syndromes, describing their clinical presentation, EEG features, treatment, prognosis, and underlying genetics. The following GGE syndromes are discussed in order of their age of onset—myoclonic astatic epilepsy, childhood absence epilepsy, epilepsy with myoclonic absences, eyelid myoclonia with absences, juvenile absence epilepsy, juvenile myoclonic epilepsy, and epilepsy with generalized tonic seizures on awakening. This is followed by an overview on pathophysiological mechanisms underlying GGE.

Clinical and genetic aspects of juvenile absence epilepsy

1994 ◽  
Vol 241 (8) ◽  
pp. 487-491 ◽  
Author(s):  
Tahir Obeid
Keyword(s):  
Absence Epilepsy ◽  
Juvenile Absence Epilepsy

scholarly journals Seizure Exacerbation by Antiepileptic Drugs

2005 ◽  
Vol 5 (5) ◽  
pp. 192-193 ◽  
Author(s):  
Jacqueline A. French
Keyword(s):  
Antiepileptic Drugs ◽  
De Novo ◽  
Focal Epilepsy ◽  
Juvenile Myoclonic Epilepsy ◽  
Absence Epilepsy ◽  
Absence Seizures ◽  
Incorrect Diagnosis ◽  
Juvenile Absence Epilepsy ◽  
Generalized Epilepsy

Worsening of Seizures by Oxcarbazepine in Juvenile Idiopathic Generalized Epilepsies Gelisse P, Genton P, Kuate C, Pesenti A, Baldy-Moulinier M, Crespel A Epilepsia 2004;45:1282–1286 Purpose Several studies have shown that carbamazepine (CBZ) may aggravate idiopathic generalized epilepsy (IGE). Oxcarbazepine (OXC) is a new drug chemically related to CBZ. We report six cases of juvenile IGE with a clear aggravation by OXC. Methods We retrospectively studied all patients with IGE first referred to our epilepsy department between January 2001 and June 2003 and treated with OXC. Results During this period, six patients were identified. All had an aggravation of their epilepsy in both clinical and EEG activities. OXC had been used because of an incorrect diagnosis of focal epilepsy or generalized tonic–clonic seizures (GTCSs) of undetermined origin (no syndromic classification of the epilepsy). Before OXC, only one patient had experienced a worsening of seizures with an inadequate drug (carbamazepine; CBZ). Four had juvenile myoclonic epilepsy, one had juvenile absence epilepsy, and one had IGE that could not be classified into a precise syndrome. OXC (dosage range, 300–1,200 mg/day) was used in monotherapy in all of them except for one patient. Aggravation consisted of a clear aggravation of myoclonic jerks (five cases) or de novo myoclonic jerks (one case). Three patients had exacerbation of absence seizures. One patient had worsened dramatically and had absence status, and one had de novo absences after OXC treatment. The effects of OXC on GTCSs were less dramatic, with no worsening in frequency in three and a slight increase in three. Conclusions OXC can be added to the list of antiepileptic drugs that can exacerbate myoclonic and absence seizures in IGE.

scholarly journals Temporal intermittent delta activity: A marker of juvenile absence epilepsy?

Seizure ◽  
2011 ◽  
Vol 20 (1) ◽  
pp. 38-41 ◽  
Author(s):  
Philippe Gelisse ◽  
Anna Serafini ◽  
Reana Velizarova ◽  
Pierre Genton ◽  
Arielle Crespel
Keyword(s):  
Absence Epilepsy ◽  
Delta Activity ◽  
Juvenile Absence Epilepsy

Juvenile Absence Epilepsy

2010 ◽  
pp. 17-20
Author(s):  
Jeffrey L. Sponsler
Keyword(s):  
Absence Epilepsy ◽  
Juvenile Absence Epilepsy

scholarly journals Generalized spike-wave discharges involve a default mode network in patients with juvenile absence epilepsy: A MEG study

2010 ◽  
Vol 89 (2-3) ◽  
pp. 176-184 ◽  
Author(s):  
Kotaro Sakurai ◽  
Youji Takeda ◽  
Naoaki Tanaka ◽  
Tsugiko Kurita ◽  
Hideaki Shiraishi ◽  
...  
Keyword(s):  
Default Mode Network ◽  
Absence Epilepsy ◽  
Default Mode ◽  
Spike Wave Discharges ◽  
Juvenile Absence Epilepsy ◽  
Spike Wave

scholarly journals An association analysis at 2q36 reveals a new candidate susceptibility gene for juvenile absence epilepsy and/or absence seizures associated with generalized tonic-clonic seizures

Epilepsia ◽  
2011 ◽  
Vol 52 (5) ◽  
pp. 975-983 ◽  
Author(s):  
Özlem Yalçin ◽  
Betül Baykan ◽  
Kadriye Ağan ◽  
Zuhal Yapici ◽  
Destina Yalçin ◽  
...  
Keyword(s):  
Association Analysis ◽  
Susceptibility Gene ◽  
Absence Epilepsy ◽  
Absence Seizures ◽  
Juvenile Absence Epilepsy ◽  
Clonic Seizures

ESP04 Juvenile absence epilepsy and juvenile myoclonic epilepsy

2007 ◽  
Vol 11 ◽  
pp. 61
Author(s):  
O. Milovanova ◽  
V. Zykov ◽  
T. Klimenko
Keyword(s):  
Juvenile Myoclonic Epilepsy ◽  
Absence Epilepsy ◽  
Myoclonic Epilepsy ◽  
Juvenile Absence Epilepsy

scholarly journals Juvenile absence epilepsy relapsing as recurrent absence status, mimicking transient global amnesia, in an elderly patient

2018 ◽  
Vol 20 (6) ◽  
pp. 557-561
Author(s):  
Lorenzo Muccioli ◽  
Laura Licchetta ◽  
Carlotta Stipa ◽  
Paolo Tinuper ◽  
Francesca Bisulli
Keyword(s):  
Elderly Patient ◽  
Transient Global Amnesia ◽  
Absence Epilepsy ◽  
Absence Status ◽  
Juvenile Absence Epilepsy ◽  
Global Amnesia
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