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Cryptogenic epilepsy: Difference between revisions
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The criptogenic epilepsy is a group of epilepsy syndromes, both focal or generalized ones, with not demonstrated ethiology by the usual laboratory or neuroimaging techniques, but which are considered to be symptomatic of a hidden histopathological or cellular alteration, but not of a genetic nature<ref>http://www.cun.es/diccionario-medico/terminos/epilepsia-criptogenica</ref><references/> | The criptogenic epilepsy is a group of epilepsy syndromes, both focal or generalized ones, with not demonstrated ethiology by the usual laboratory or neuroimaging techniques, but which are considered to be symptomatic of a hidden histopathological or cellular alteration, but not of a genetic nature<ref>http://www.cun.es/diccionario-medico/terminos/epilepsia-criptogenica</ref> | ||
==Links== | |||
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1718261/pdf/v082p00226.pdf Diagnosing idiopathic/cryptogenic epilepsy syndromes in infancy | |||
<references/> | |||
Revision as of 17:36, 12 December 2016
The criptogenic epilepsy is a group of epilepsy syndromes, both focal or generalized ones, with not demonstrated ethiology by the usual laboratory or neuroimaging techniques, but which are considered to be symptomatic of a hidden histopathological or cellular alteration, but not of a genetic nature[1]
Links
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1718261/pdf/v082p00226.pdf Diagnosing idiopathic/cryptogenic epilepsy syndromes in infancy