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indian/seizures

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Epilepsy: Indian perspective.

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There are 50 million people living with epilepsy worldwide, and most of them reside in developing countries. About 10 million persons with epilepsy are there in India. Many people with active epilepsy do not receive appropriate treatment for their condition, leading to large treatment gap. The lack

Indian red scorpion envenoming.

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The clinical course and treatment outcome of scorpion envenoming in 293 children was studied in a hospital at Mahad in Raigad district of Maharastra. 111 (38%) children who reported 1-10 hours (mean 3.5 hours) after sting had hypertension, 87 (29.6%) with tachycardia reported within 1-24 hours (mean

Seizure disorders-views of the Indian medical systems.

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The deschptions, etio-pathology and some aspects of treatment of the seizure disorders in the three Indian Systems of Medicine, namely The Siddha, The Ayurveda and The Unani are briefly mentioned. "If more or less, three humors cause disease, The learned count the wind is the first of

Pediatric epilepsy - an Indian perspective.

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Prevalence studies from India suggest that epilepsy prevalence is similar to developed nations. Neurocysticercosis (NCC) predominates as an etiology. A large treatment gap is still a public health problem. Benign epilepsies and West syndrome appear to be underrepresented in studies on classification

Pediatric epilepsy -- an Indian perspective.

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Prevalence studies from India suggest that epilepsy prevalence is similar to developed nations. Neurocysticercosis (NCC) predominates as an etiology. A large treatment gap is still a public health problem. Benign epilepsies and West syndrome appear to be underrepresented in studies on classification

Epidemiology of epilepsy--Indian perspective.

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There are about 20 epidemiological studies on epilepsy from different parts of India. They include both rural and urban studies. The prevalence rate stands at around 5/1000 population (at this rate present estimate of total epileptics in this country is about 5 million) and incidence rate varies

Wilson's disease: An Indian perspective.

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Wilson's disease (WD) is an autosomal recessive disease involving a defect of copper transport by the hepatic lysosomes. It leads to excess copper deposition in the liver, the brain, the kidneys and the skeletal system, affecting most commonly children or young adults and running an invariably fatal

A study of nonepileptic seizures in an Indian population.

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OBJECTIVE The goal of this study was to evaluate the background and the clinical profile of nonepileptic seizures (NESs) confirmed by short-term video encephalography (ST-VEEG) recording in an Indian population. METHODS Seventy-one patients with NESs were enrolled. A complete history was taken and

Neuroimaging abnormalities in Indian patients with uncontrolled partial seizures.

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In this series we performed clinical and imaging evaluation of 77 consecutive patients with uncontrolled partial seizures. Single cerebral parenchymal calcification (22 patients) was the most common imaging abnormality. Nine patients had multiple punctate calcifications. Other CT abnormalities

Neck myoclonia with absence seizures in an Indian girl.

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Absence seizures associated with myoclonic phenomena have been associated with 4 seizure types. Recently, a new seizure type of neck myoclonia with absences was described. We present a case of 9-year-old girl who presented with abnormal head shaking and vacant stare for the past 5 months with an

Seizure worsening with topiramate amongst Indians with refractory epilepsy.

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In a prospective open label add-on study on 95 patients (age 1-63 years, mean 17.76 +/- 13.83 years) with seizures refractory to conventional antiepileptic drugs (AEDs) and other new AEDs, the addition of Topiramate (TPM) resulted in seizure worsening in 18 patients (19%) necessitating drug

Analbuminemia in an American Indian girl.

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Analbuminemia was fortuitously detected in a nonedematous 12-year-old American Indian girl with atopic dermatitis, mild bronchial asthma, a mild seizure disorder, and hyperlipoproteinemia with a corneal arcus. Immunologic methods revealed trace amounts (17 mg/100 ml) of apparently normal serum

Seizures among families of Indian probands with different epileptic syndromes.

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OBJECTIVE To investigate the contribution of hereditary factors in the causation of different epilepsy syndromes. METHODS Occurrence of seizures among first- and second-degree relatives of 5628 Indian probands with epilepsy, and 3357 probands with non-epilepsy neurological disorders (who acted as

Neurocysticercosis in a north Indian hospital.

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In endemic regions, neurocysticercosis (NCC) is the most commonly diagnosed parasitic disease of the central nervous system, and the most common cause of convulsions and hydrocephalus in adults. During January 2000-December 2006, serum samples collected from patients presenting with various

Prevalence of photosensitivity--an Indian experience.

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One thousand nine hundred and forty newly recruited entrants for training as pilots (Group A) underwent photic stimulation during EEG recording during the entrance examination to the flying stream. One hundred and sixty individuals (Group B) working on radars for prolonged periods were interviewed
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