Gastaut type-idiopathic childhood occipital epilepsy and childhood absence epilepsy: A clinically significant association?
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چکیده
منابع مشابه
Gastaut type-idiopathic childhood occipital epilepsy and childhood absence epilepsy: A clinically significant association?
We report an unusual association between idiopathic occipital epilepsy and childhood absence epilepsy in 2 pediatric patients. At first clinical and electroencephalographic evaluation, the patients presented the peculiar signs of idiopathic occipital epilepsy Gastaut type: focal sensory visual seizures, migraine-like symptoms (only in one patient) and unilateral spike-wave discharges over occip...
متن کاملEEG in childhood absence epilepsy
UNLABELLED We performed a longitudinal clinico-electroencephalographic study of 23 children who were diagnosed as having absence epilepsy on their initial visits to our facility and we analysed those factors which lead to an unfavourable prognosis. SUBJECTS AND METHODS We divided the 23 patients into three groups according to their clinical courses: Group A: eight patients who responded well ...
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West Syndrome (WS) is a severe epileptic encephalopathy occurring in the first year of life. According the ILAE classification of epileptic seizures and epilepsy the etiology could be symptomatic or cryptogenic. Some authors identified a small group of patients (5%) with a particular good outcome, a complete recovery from seizures and a normal cognitive development within the cryptogenic group ...
متن کاملClinical dissection of childhood occipital epilepsy of Gastaut and prognostic implication.
BACKGROUND AND PURPOSE Our aim was to describe the clinical and electrical features and the long-term evolution of childhood occipital epilepsy of Gastaut (COE-G) in a cohort of patients and to compare long-term prognosis between patients with and without other epileptic syndromes. METHODS This was a retrospective analysis of the long-term outcome of epilepsy in 129 patients with COE-G who we...
متن کاملBenign myoclonic epilepsy in infancy followed by childhood absence epilepsy
Benign myoclonic epilepsy in infancy (BMEI) is a rare syndrome included among idiopathic generalized epilepsies (IGE) and syndromes with age-related onset. Recently, it has been shown that a few patients with BMEI later had other epilepsy types mainly IGE but never childhood absence epilepsy (CAE). We report a patient who at 11 months of age showed isolated myoclonic jerks occurring several tim...
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ژورنال
عنوان ژورنال: Seizure
سال: 2010
ISSN: 1059-1311
DOI: 10.1016/j.seizure.2010.04.010