Document Detail

Absence seizures in the first 3 years of life: An electroclinical study of 46 cases.
MedLine Citation:
PMID:  21269284     Owner:  NLM     Status:  Publisher    
Purpose:  Early onset absence seizures have been considered a rare heterogeneous group with a poor prognosis. Only few patients may be categorized into well-known syndromes. We have evaluated electroclinical features, evolution, and the nosologic boundaries of early onset absence seizures. Methods:  Forty-six neurologically normal patients with absence seizures associated with bilateral, synchronic, or asynchronic, and symmetric or asymmetric spike-and-wave paroxysms with onset in the first 3 years of life were included. Patients with abnormal neurologic examination and brain imaging were excluded from the study. Key Findings:  In our study, 39 patients met the clinical and electroencephalography (EEG) criteria of well-defined epileptic syndromes. Childhood absence epilepsy was found in 11 patients, benign myoclonic epilepsy in infancy in 18 patients, eyelid myoclonic epilepsy in 4, and epilepsy with myoclonic absences in 6. We did not find clinical and EEG criteria of well-recognized epileptic syndromes in seven children. Nine of 11 patients with simple absence seizures became seizure free. All these patients had normal neurologic and neuropsychological evaluations. Of the 35 patients who had absence seizures associated with myoclonic seizures, 20 became seizure free. Fifteen of 35 children continue having seizures. At the last visit, 20 of these 35 patients had normal neurologic and neuropsychological evaluations, 11 presented with mild mental retardation, and 4 with severe mental retardation. Significance:  Epilepsies with absence seizures of early onset are relatively uncommon. Most of the patients had well-defined epileptic syndromes with a variable evolution. The evolution depended on the epileptic syndromes.
Roberto Horacio Caraballo; Francesca Darra; Elena Fontana; Roberto Garcia; Eduardo Monese; Bernardo Dalla Bernardina
Related Documents :
1477624 - Cone dystrophies: clinical and electrophysiological findings.
6493704 - Grating and recognition acuities of pediatric patients.
7945034 - Treatment of acquired nystagmus with botulinum neurotoxin a.
19834404 - Stereotactic radiosurgery for cavernous sinus or orbital hemangiomas.
2486594 - Precordial doppler monitoring and pulse oximetry during cesarean delivery: detection of...
3956524 - An implantable antitachycardia pacemaker with back-up pacing and scanning burst mode.
Publication Detail:
Type:  JOURNAL ARTICLE     Date:  2011-1-26
Journal Detail:
Title:  Epilepsia     Volume:  -     ISSN:  1528-1167     ISO Abbreviation:  -     Publication Date:  2011 Jan 
Date Detail:
Created Date:  2011-1-28     Completed Date:  -     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  2983306R     Medline TA:  Epilepsia     Country:  -    
Other Details:
Languages:  ENG     Pagination:  -     Citation Subset:  -    
Copyright Information:
Wiley Periodicals, Inc. © 2011 International League Against Epilepsy.
Department of Neurology, Hospital Nacional de Pediatría "Prof Dr Juan P Garrahan," Buenos Aires, Argentina Neuropsichiatria Infantile, Ospedale Gianbattista Rossi, Università di Verona, Verona, Italia.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine

Previous Document:  Cognitive development in Dravet syndrome: A retrospective, multicenter study of 26 patients.
Next Document:  Comorbidities of epilepsy: Results from the Epilepsy Comorbidities and Health (EPIC) Survey.