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Abstract Convulsive phenomena are one of the most common neurologic problem in children. A seizure is the clinical manifestation of an abnormal neuronal hyperactivity which usually involve cerebral cortical neurons, primarily or secondarily, and is manifested in a manner dependent upon the extent and location of this neuronal hyperactivity. Classification of epileptic seizures is still a problem. There is a difficulty of devising a single code to COver three basically incompatible systems of classification, ~elating to the clinical features of the fit, to the anatomical and electrophysiological evidence of the source of the fit, and to its aetiology when known. Causes of convulsive seizures are different for each childhood age group. In the neonatal period; convulsions are due to metabolic disorders, intracranial birth injury, intracranial infections, congenital cerebral malformations, drugs, and developmental abnormalities. Perinatal hypoxia and intracranial haemorrhage are the most common causes of neonatal convulsions and these account for over 50% of seizures in the neonatal period. In infancy, congenital abnormalities of the brain are a very common cause of convulsions specially between the age of 2 months and 6 months and acute infections specially meningitis also become significant. Febrile seizures are those occuring in children in association with fever and clinical illness other than those involvi~ ng the brain. Seizures occur between the age of 3 months and 5 years with an incidence of 3-4% of all children. In childhood, idiopathic cause of convulsion. epilepsy is Other causes the most common include: trauma, toxic reactions and poisoning, and vascular causes as hypertensive encephalopathy. Classification of epileptic: seizures is based on the most recent internationally revised classification produced in 1981. This new classification subdivide seizures on the basis of the clinical features of these seizures and the ictal and interictal electroencephalographic features. There are two basic types of seizures, partial and generalized seizures. Partial seizures are the manifestation of a focal epileptic discharge in only a portion of the brain. These seizures are classified on the basis of whether or not consciousness is impaired during the attacks. When consciousness is not impaired, the seizure is classified as a simple partial seizure and when consciousness is impaired, the seizures is classified as a complex partial seizure. In generalized seizures, motor signs are bilateral and reflect neuronal discharges that are widespread in both hemispheres. These types of seizures include: absence, myoclonic, clonic, tonic, tonic-clonic, and atonic seizures. Management of consists of two 2) therapy with a child with convulsive disorders phases: 1) aetiologic delineation; removal of the specific cause or suppresion of seizures with anticonvulsants. Laboratory examinations include: EEG, roentgenogram, CSF examination, blood studies for electrolyte assessment, blood picture and culture, and urine analysis for heavy metals, drugs and amino acid analysis. The advent of computerized tomography has helped greatly in the investigation of epileptic seizures. Approximately 50% of patients with focal signs and symptoms and abnormal focus on EEG had abnormal CT scan. The objective in the treatment of epileptic patients is complete control of seizures, or at least reduction in their frequency to the point at which they no longer interfere with the physical and social well-being.Emerg_ ency management of neonatal seizures includes a trial to corret the metabolic deficiency until biochemical and metabolic disorders are excluded. In a child with febrile convulsion, fever should be reduced by tepid water and antipyretics, and treatment of the causative infection is essential. Phenobarbitone, diphenYlhYdantoin (epanutin), and primidone are most often used for generalized tonicclonic seizures and partial seizures. EthosUximide is very effective in reducing petit mal (absence) seizures and excellent results have also been found with valproic acid. Once seizures are contrOlled, the anticonvulsant drug should be continued for a prolonged period without altering its dosage. Generally, children with epilepsy should be treated for at least 4 seizurefree years before drug withdrawal. |