نتایج جستجو برای: gastaut syndrome lgs

تعداد نتایج: 622374  

Journal: :Archives of disease in childhood 1979
R Biagini R Tignani A R Fifi L Nappini

A 14-year-old boy had suffered from intermittent acute hepatic porphyria, myoclonic convulsions and mental retardation (Lennox-Gastaut syndrome). The porphyria was treated by stopping the administration of phenobarbitone and phenytoin. Sodium valproate at a dose of 70 mg/kg per day lessened the severity and frequency of convulsive crises.

Journal: :Epilepsy research 1999
A Kaminska A Ickowicz P Plouin M F Bru G Dellatolas O Dulac

PURPOSE To distinguish various types of childhood severe cryptogenic/idiopathic generalised epilepsy on the basis of reproducible diagnostic criteria, using multiple correspondence analysis (MCA). METHODS We applied MCA to a series of 72 children with no evidence of brain damage, starting epilepsy between 1 and 10 years, with two or more types of generalised seizures. We excluded patients wit...

Journal: :Zeitschrift Für Epileptologie 2022

Abstract Down syndrome (DS) is the most common cause of intellectual disability. Due to many genetic and biochemical aberrations, people with DS suffer from several somatic disorders concomitant diseases. Epilepsies occur more often than in normal population, but less disability other causes. have a trimodal distribution age-related phenotypes, etiologies, prognosis. The epilepsy infancy often-...

Journal: :Neurology 2003
Y Takahashi H Mori M Mishina M Watanabe T Fujiwara J Shimomura H Aiba T Miyajima Y Saito A Nezu H Nishida K Imai N Sakaguchi N Kondo

BACKGROUND Antibody-mediated and cytotoxic T cell-mediated pathogenicity have been implicated as the autoimmune pathophysiologic mechanisms in Rasmussen's encephalitis. METHODS The authors investigated autoantibodies against the NMDA glutamate receptor (GluR) epsilon2 subunit and their epitopes in serum and CSF samples from 15 patients with chronic epilepsia partialis continua (EPC), 17 with ...

2017
Carla Marini Michele Romoli Elena Parrini Cinzia Costa Davide Mei Francesco Mari Lucio Parmeggiani Elena Procopio Tiziana Metitieri Elena Cellini Simona Virdò Dalila De Vita Mattia Gentile Paolo Prontera Paolo Calabresi Renzo Guerrini

Objective To describe electroclinical features and outcome of 6 patients harboring KCNB1 mutations. Methods Clinical, EEG, neuropsychological, and brain MRI data analysis. Targeted next-generation sequencing of a 95 epilepsy gene panel. Results The mean age at seizure onset was 11 months. The mean follow-up of 11.3 years documented that 4 patients following an infantile phase of frequent se...

Journal: :Journal of clinical neurophysiology : official publication of the American Electroencephalographic Society 2006
Richard A Hrachovy James D Frost

This article reviews the ictal and interictal EEG findings associated with a select group of generalized seizures. These include absence seizures, myoclonic seizures seen in juvenile myoclonic epilepsy, idiopathic generalized tonic clonic seizures, infantile spasms, and atypical absence, tonic, and atonic seizures associated with the Lennox Gastaut syndrome.

Journal: :Journal of neurology, neurosurgery, and psychiatry 1986
R D Rafal K D Laxer J S Janowsky

An epileptic girl with Lennox-Gastaut syndrome had seizures triggered specifically by blinking, but not by other eye movements or by photic stimulation. Electrographic and clinical seizures were most reliably precipitated by repetitive blinking produced voluntarily on command, by reflex blinking on corneal stimulation, or by psychogenic triggers of blinking such as social stress or cognitive ef...

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