dementia/crise épileptique

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Cobalamin deficiency manifested with seizures, mood oscillations, psychotic features and reversible dementia in the absence of typical neurologic and hematologic signs and symptoms: a case report.

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Cobalamin deficiency is associated with a wide spectrum of hematologic, neurologic, gastroenterologic and psychiatric disorders or symptoms. We report a case of a 50-year-old man with complex partial seizures with secondary generalization, mood oscillations and psychotic symptoms alternating with

Dementia, delusions and seizures: storage disease or genetic AD?

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We describe a case of a young patient suffering from a rapidly progressive cognitive decline, associated with delusions, myoclonus and seizures and with no family history for dementia. Clinical features, along with skin biopsy findings were overlapping storage disease; the genetic analysis, however,

Intraventricular haemorrhage and seizures in a patient with dementia: a case of chronic neurobrucellosis.

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Brucellosis is the most commonly reported zoonosis. Nervous system participation can occur at any stage of the disease either in acute or subacute or chronic form. Isolated nervous system involvement or neurobrucellosis is a relatively rare form of the disease. We describe an unusual case of an

[Spontaneous seizures improve severe dementia conditions. Dementia contra depression-induced pseudodementia and electric stimulation therapy of depressed patients with epilepsy].

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On the basis of two case reports, the differential diagnostic difficulties between pseudodementia conditioned by depression and genuine dementia are discussed and the particular conditions present in connection with electroconvulsive therapy (ECT) in patients with reduced seizure thresholds.

Epileptic seizure presenting as dementia with Lewy bodies.

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Psychotic symptoms and cognitive fluctuation are common manifestations of dementia with Lewy bodies (DLB). However, the differentiation of these symptoms is difficult because many psychiatric, neurologic, and medical conditions in addition to drug effects can mimic DLB in elderly people. We report

Reversible dementia: subclinical seizure in early-onset dementia.

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We report a case of early-onset dementia with subclinical seizures. Aggressive seizure control improved the patient's cognition. Commonly, an EEG is only performed following overt behavioral seizures. Therefore, subclinical seizures tend to be underdiagnosed. Serial or extended EEG should be

Complex partial seizures presenting as frontotemporal dementia: a case report.

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Both epilepsy and dementia are common after the age of 65. Epilepsy, originating in the temporal lobes, can present clinically in a variety of ways and can be difficult to diagnose. Loss of consciousness may not be evident. Reported here is a unique case of a 65 year old man who presented with

Seizures and early onset dementia: D2HGA1 inborn error of metabolism in adults

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D-2-hydroxyglutaric aciduria type 1 (D2HGA1) is a rare inherited metabolic disorder usually manifesting in infancy/early childhood with seizures and significant central nervous system involvement. We report two siblings with D2HGA1 presenting with mild intellectual disability, and the onset of

Hyperexcitability and epileptic seizures in a model of frontotemporal dementia.

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Epileptic seizures are more common in patients with Alzheimer disease than in the general elderly population. Abnormal forms of hyperphosphorylated tau accumulate in Alzheimer disease and other tauopathies. Aggregates of tau are also found in patients with epilepsy and in experimental models of

Early epileptic seizures after stroke are associated with increased risk of new-onset dementia.

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BACKGROUND Subclinical vascular or degenerative lesions occur in the brain before the clinical expression of dementia. Those lesions in a brain that just experienced a stroke may have lower thresholds for early epileptic seizures. Therefore, epileptic seizures may be a marker of subclinical brain

Early-onset dementia with prolonged occipital seizures: an atypical case of Kufs disease.

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OBJECTIVE Kufs disease is the adult-onset form of neuronal ceroid lipofuscinosis (NCL). Its two clinical phenotypes are type A (progressive myoclonus epilepsy with dementia) and type B (behavioral abnormalities and dementia, associated with pyramidal and extrapyramidal signs). METHODS We describe

[A 85-year-old woman with one year history of convulsion, dementia, and consciousness disturbance].

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We report a 85-year-old woman who died after one year history of convulsion, dementia, and consciousness disturbance. She was apparently well until January 6, 1995 when she was 85 year old; on that evening, she suddenly stated that some one was in her room and she became confused. A local MD gave

Influence of pre-existing dementia on the risk of post-stroke epileptic seizures.

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BACKGROUND Seizures occur in 10% of stroke patients, but their predictors have not been clearly identified. Pre-existing dementia is present in 12-16% of stroke patients and, at the community level, patients with dementia have increased risk of seizures. However, the question of whether pre-existing

[A 83 year-old woman with dementia, gait disturbance, and convulsion].

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We report a 83 year-old woman with dementia. She was apparently well until December of 1993 when she was 81-year-old. At that time, she was operated or her cataract. Her post operative course was uneventful, however, shortly after her operation, she had an onset of memory loss and abnormal behavior.

Dementia with Lewy bodies presenting as probable epileptic seizure.

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We discuss the case of an 83-year-old man admitted to the hospital after losing control of his vehicle due to an unexplained episode of altered consciousness. This occurred on a background of multiple similar episodes associated with acute confusion, superimposed on a gradual cognitive decline

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