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neuritis/crise epiléptica
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Psychosocial and seizure factors related to depression and neurotic-disorders among patients with chronic epilepsy in Nigeria.
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To establish the effect of psychosocial and seizure factors on Depression and Neurotic Disorders among clinically diagnosed Nigerian patients, with epilepsy. This study utilized the multivariate statistical design to evaluate the associations between some psychosocial and seizure factors on increase
[Convulsive seizures and polyneuritis in a patient with lupus treated with metronidazole (author's transl)].
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A 20-year-old patient with biologically-confirmed lupus developed a perirenal abscess following puncture biopsy of the kidney. Postoperative treatment included metronidazole at a mean dose of 2.5 g daily for 68 days (total dose : 165 g). Generalised convulsive seizures occurred on four occasions,
Anti-myelin oligodendrocyte glycoprotein (MOG) antibodies in patients with optic neuritis and seizures.
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We describe four patients who experienced optic neuritis (ON) and seizures and were found to have antibodies to myelin oligodendrocyte glycoprotein (MOG) in serum. The index case was a previously healthy 39-year-old man who developed steroid dependent ON and had a generalized seizure when steroids
[Metronidazole-related polyneuritis, convulsive seizures, and cerebellar syndrome. Contribution of MRI].
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BACKGROUND
Neurological complications of metronidazole are rare, predominantly peripheral neuropathies, especially in patients on a long-term high-dose regimen. Cerebellar syndrome or seizures are less frequently reported. The concomitant occurrence of the three complications is
[Studies on mechanism of psycho-neurotic disturbances caused by INAH administration. I. On the relationship between INAH metabolism and convulsion caused by INAH administration].
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[Experimental neurotic convulsions].
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Seizures and retrograde amnesia with cerebrospinal fluid changes following H1N1 influenza vaccination.
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Vaccination against H1N1 influenza of healthcare workers of has been a standard measure to control the epidemic in many countries. Most side effects are minor and transient. Guillain Barre Syndrome and optic neuritis have been major concerns. We report a case of seizures with retrograde amnesia
[Significance of serum prolactin determination in the differential diagnosis of psychogenic seizures--exemplified by 2 case reports].
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Conversion neurotic bodily disorders manifest themselves mainly in the motor system (e.g. psychogenic paralyses and gait disturbances). Psychogenic seizures are observed as well; these may also become manifest as hystero-epilepsy association with an organic convulsive disease. The described symptoms
Bilateral postinfectious optic neuritis and intravenous steroid therapy in children.
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Six patients presented with acute, simultaneous, bilateral optic neuritis. Five of the six patients admitted to a recent history of a brief upper respiratory or gastrointestinal illness, presumably viral in nature. Visual acuity was severely reduced in all patients. Five of the six patients also
[A case of anti-myelin oligodendrocyte glycoprotein (MOG) and anti-N-methyl-D-aspartate (NMDA) receptor antibody-positive encephalitis with optic neuritis].
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A 20-year-old female was hospitalized due to generalized seizure two weeks after an infection. She reported disorientation, neck stiffness and weakness in her legs. MRI FLAIR images and T2WI on her first visit to our hospital showed hyperintense lesions in the bilateral cingulate gyrus and the
[Torticollis and seizures due to neuroborreliosis in a child].
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BACKGROUND
In children, neuroborreliosis often manifests itself as cranial neuritis (particularly facial palsy) or aseptic meningitis. Presentation with torticollis and simple partial seizures resulting from diffuse leptomeningeal inflammation is rare.
METHODS
A seven-year-old boy who had developed
Psychical and psychological characteristics of patients with nonepileptic seizures.
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OBJECTIVE
To explore psychic and psychological characteristics of patients suffering from non- epileptic seizures and compare them with the patients suffering from epilepsy.
METHODS
Using medical documentation 40 patients with non epileptic seizures were compared with 40 randomly selected epilepsy
[Idiopathic plasmacytic lymphadenopathy with polyclonal hyperimmunoglobulinemia in a patient who died of progressive peripheral polyneuritis and cerebral dysfunction].
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We reported a 59-year-old woman who received a diagnosis of psoriasis vulgaris at the age of 35 and had been under medical treatment. She was admitted to our department on August 16, 1993 because of lymphadenopathy, arthralgia and neuralgia. We observed cervical and axillar lymphadenopathy 1-3 cm in
Anti-myelin oligodendrocyte glycoprotein (MOG) antibodies in a Japanese boy with recurrent optic neuritis.
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BACKGROUND
Myelin oligodendrocyte glycoprotein (MOG) localizes on the outermost surface of the myelin sheath and oligodendrocytes in the central nervous system (CNS). Autoantibodies against MOG are reportedly found in patients with spectrum of inflammatory demyelinating diseases of the CNS,
Peripheral neuritis in psittacine birds with proventricular dilatation disease.
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Necropsies were performed on 14 psittacine birds of various species suspected to have proventricular dilatation disease (PDD). Eight of the birds exhibited neurological signs (seizures, ataxia, tremors and uncoordinated movements) and digestive tract signs (crop stasis, regurgitation, inappetance
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