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Query: UMLS:C0036572 (seizures)
 80,221 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

In a retrospective study of 30 Down syndrome (DS) patients with epilepsy, we found 6 cases (20%) with reflex seizures. One patient had benign myoclonic epilepsy of infancy with clinical photosensitivity. The other 5 cases had all startle-induced epileptic seizures and a form of symptomatic epilepsy. Three patients had a Lenox-Gastaut syndrome, one had generalized symptomatic epilepsy, and one had partial symptomatic epilepsy (PSE). Reflex epilepsy was also used as a classification category in the PSE case, as most or all seizures were stimulus-related in this patient. Seizures precipitated by stimuli were stereotyped in 4 patients, but 2 patients responded to stimuli with different types of seizures. The actual occurrence of reflex seizures in DS patients with epilepsy is probably underestimated. These cases seem to confirm previous reports showing deficiencies in cortical inhibition in the brain of DS patients.
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PMID:Reflex seizures are frequent in patients with Down syndrome and epilepsy. 214 49

Thirty-four adolescents with epilepsy, controls matched for age and sex (A) and controls matched for age, sex and general ability (B), were studied. The adolescents with epilepsy were more likely to arrive at school by car or taxi and to have more difficult behaviour in class. Competitive sports were less popular with them and significantly fewer anticipated ever driving a car. Illness and parental marital problems were not a feature of their families. Their comprehension of reading material was significantly poorer than that of control group A. Within the group, the lowest over-all reading scores were found in children with myoclonic seizures, partial seizures with secondary generalisation, or generalised tonic-clonic seizures; and in those whose EEG findings included two-per-second spike and wave, photosensitivity, generalised slow waves, or generalised spike and wave of non-specific frequency. Right focal slow waves, sharp waves and spikes on EEG were associated with problems of comprehension, even when the over-all reading score was acceptable.
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PMID:A survey of adolescents with epilepsy. 225 83

A retrospective study was performed on 34 patients with photosensitivity detected on the electroencephalogram. This group was compared to an aleatory sample, with 218 patients. The objectives were to evaluate the photosensitivity and: type of epilepsy, age of onset of seizures, sex ratio, frequency of seizures, and family history.
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PMID:[Photosensitivity in primary and secondary epilepsies]. 226 Sep 50

The present study is based on the data of a more extensive investigation of the genetics of spike-wave epilepsies of childhood with minor seizures (Doose and Baier 1987). It evaluated EEG findings in 271 siblings of patients by means of log-linear methods. The risk of siblings to manifest spikes and waves during rest or hyperventilation is distinctly increased if they are positive for 4-7 Hz rhythms, and to a lesser degree, if they are photosensitive. Moreover, siblings of female patients seem to be at a higher risk of manifest spikes and waves than siblings of males. 4-7 Hz rhythms of the EEG background activity and photosensitivity are mutually independent symptoms of an increased liability to manifest spikes and waves. These findings are discussed in the context of a 'multifactorial' background of spikes and waves.
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PMID:Interdependence of different genetic EEG patterns in siblings of epileptic patients. 243 13

We report the EEG changes that occurred on discontinuance of phenytoin (PHT), carbamazepine (CBZ), and valproate (VPA) in patients with active epilepsy. Discontinuation of CBZ was associated with an increase in mean frequency of dominant rhythm and reduction in amount of slow activity. Patients who had a marked increase in seizures on discontinuation of an antiepileptic drug had a slower mean dominant rhythm at baseline than did patients who did not have an increase in seizures. Subsequent EEGs, during and at the end of drug reduction, showed an increase in bursts of interictal epileptiform activity (IEA) and in slow activity in patients who had a marked increase in seizures. The amount of slow activity and IEA did not alter in patients who did not have an increase in seizures. No patients developed photosensitivity.
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PMID:Effects of the removal of phenytoin, carbamazepine, and valproate on the electroencephalogram. 250 4

The electroencephalograms (EEGs) of 22 patients suffering from hereditary DRPLA were studied. Epileptoform patterns were observed in 14 patients (63.6%) with epileptic seizures. The epileptoform patterns most frequently observed were those atypical spike-wave complexes. Slow wave bursts were seen in 18 patients (81.8%). Photosensitivity was revealed in six (27.3%) patients, all of whom presented progressive myoclonus epilepsy (PME) syndrome. Abnormal background activity was evident in 17 (77.3%) patients. These abnormalities in EEG were more severe in patients in the PME type than those of the A (ataxia) and AE (ataxia and epilepsy) types.
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PMID:Electroencephalographic findings of hereditary dentatorubral-pallidoluysian atrophy (DRPLA). 252 87

Photosensitivity is a rare phenomenon found, often more or less accidentally, in approximately 5% of epileptic patients. Its pathophysiology still remains largely unsolved and the clinical significance of photosensitivity is controversial. The literature on the subject is impressive, yet predominantly anecdotal. In this thesis we describe the results of an extensive and standardized study of 100 consecutive photosensitive patients with special emphasis on the clinical history, the seizure history and the electrophysiological findings. These are then compared to identical data of an age and sex matched control group, obtained from the same population of epileptic patients, referred to a special (tertiary care) epilepsy clinic. In chapter I, the literature is reviewed and photosensitivity as a special form of "reflex epilepsy" is discussed. A distinction is made between normal and abnormal reactions on intermittent photic stimulation (IPS) during electroencephalographic (EEG) registrations and the criteria of true photosensitivity are formulated. The relation between the presence of photosensitivity during EEG examination and the occurrence of visually-induced epileptic seizures in daily life is discussed. As self-induction of seizures has been associated with photosensitivity, an extensive review, including a special reference list (see appendix A), is given concerning such self-inducing behaviour in photosensitive patients. A review of photosensitivity as a genetic marker and model of epilepsy concludes this chapter. In chapter II the aims of this study are outlined. Some general conceptions about photosensitive epilepsy have become widely accepted in clinical practice without much scientific support, i.e., the idea that the finding of photosensitivity is synonym with the diagnosis of primary generalized epilepsy. Furthermore, photosensitivity is generally believed to be a genetically determined, benign type of epilepsy in childhood and adolescence but when associated with self-inducing behaviour is interpreted as a sign of mental subnormality. Whether or not these conceptions are valid and whether photosensitivity is or is not a special subtype of epilepsy remains unsolved. In this study we thus set out to answer the following questions: A. Are photosensitive epileptic patients different from non-photosensitive patients with epilepsy, with respect to clinical history and, more specifically, to seizure history and family history for seizures? B. Is the degree of photosensitivity, established as photosensitivity range, predictive for the liability to visually-induced seizures in daily life? Are detailed laboratory findings concerning sensitivity to television and black-and-white striped patterns of clinically predictive value, e.g. can patients, liable to TV epilepsy or pattern-induced seizures, be identified by EEG investigations?
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PMID:Photosensitivity in epilepsy. Electrophysiological and clinical correlates. 261 89

Thirteen patients with dyssynergia cerebellaris myoclonica (Ramsay Hunt syndrome) had full clinical and neurophysiological study as well as muscle biopsy. The patients had action myoclonus, generalised epileptic seizures, and mild cerebellar syndrome. The disease was inherited in an autosomal recessive pattern in five patients, and occurred as isolated cases in the remaining eight patients. The age at onset of symptoms ranged from 6 to 15 years (mean, 10.4 years). The EEG and polygraphic findings included normal background activity in most patients, spontaneous fast generalised spike-and-wave discharges, photosensitivity, no activation during slow sleep, and vertex and rolandic spikes in REM sleep. Results of muscle biopsy, performed an average of 14 years after onset of the disease, were normal and showed no mitochondrial abnormalities. These findings suggest that Ramsay Hunt syndrome is a condition with distinctive clinical and neurophysiological features and unrelated to mitochondrial encephalomyopathies.
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PMID:Dyssynergia cerebellaris myoclonica (Ramsay Hunt syndrome): a condition unrelated to mitochondrial encephalomyopathies. 210 13

Rhythmic theta activity maximally expressed in the parietobasal leads is a characteristic interictal EEG pattern in infants and children with primarily generalized "corticoreticular" seizures, including febrile convulsions. It is a strictly age-dependent electroencephalographic expression of a widespread genetic disposition to convulsions. If it coincides with photosensitivity, it leads to a considerable risk of spikes and waves. As epidemiological and family studies have shown, it is most likely polygenically determined and genetically independent of both photosensitivity and focal sharp waves. In epileptic patients the persisting expression of parietal theta rhythms beyond childhood bears prognostic significance. As one among many factors the "theta trait" is of importance in the "multifactorial" pathogenesis of epilepsy.
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PMID:Theta rhythms in the EEG: a genetic trait in childhood epilepsy. 306 27

Since 1968, annual EEG recordings during photic stimulation using a standardised technique have been made on photosensitive patients and siblings. In 1983, 72 were aged greater than or equal to 20 years and 14 were aged 16-19 years. Mean duration of follow-up was 9.8 +/- 4.8 years. Seventy-five patients were treated with sodium valproate (VPA), which was withdrawn in 15 but restarted in eight because of return of photosensitivity. Eighty-two patients had seizures at some time; at follow-up 58 were receiving monotherapy with VPA, seven were receiving comedication, and three were taking other drugs. Fifty-four of them were seizure free, as were 10 of the 15 who were not being treated with drugs. Photosensitivity disappeared in 44 of 65 patients at a mean dosage of VPA at 21.5 +/- 6 mg/kg day. In 55 of 86 patients photosensitivity was no longer present at follow-up; in 18, slight abnormality was evoked by intermittent photic stimulation, and in 13, photoconvulsive responses were still present. Eighteen patients were not receiving drugs, 10 of them being no longer photosensitive at the mean age of 24.5 +/- 4.9 years. Thirty-one treated and untreated patients were still photosensitive at age 21.5 +/- 3.4 years. Photosensitivity disappeared earlier in those treated with VPA than in the untreated. Spontaneous remission in the treated cases may have occurred at 22.9 +/- 2.5 years of age. Photosensitivity appears around puberty and may disappear around 24 years of age. Photosensitive epilepsy is easily and rapidly controlled by VPA.
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PMID:The prognosis of photosensitivity. 309 15


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