WebWest syndrome is an epileptic encephalopathy characterized by epileptic spasms, a specific pattern on electroencephalography of hypsarrhythmia, and developmental regression. Our aim was to assess white matter abnormalities in West syndrome of unknown etiology. WebAug 1, 2014 · West syndrome is an age-dependent epileptic encephalopathy characterized by epileptic spasms and the specific interictal electroencephalography (EEG) abnormality …
West’s Syndrome: Causes, Symptoms, Treatment, Life …
WebMar 1, 2007 · Cryptogenic West syndrome was defined according to the following criteria: (1) clusters of epileptic spasms with onset <3 years, (2) hypsarrhythmia on electroencephalography (EEG), (3) normal pregnancy, normal development and no eventful history (including no other type of seizures before onset of spasms), (4) no focal … WebMay 1, 2013 · Infants with West syndrome without identification of underlying neurological disorder after adequate investigations are classified as “cryptogenic” and usually have better prognoses than children with “symptomatic” West syndrome. 1 Early seizure cessation, particularly among cryptogenic cases, may cure the disease and allow a good ... pant evisu
PET in Infancy Predicts Long-Term Outcome during Adolescence …
WebThe clinical and electroencephalographic data of 31 children with cryptogenic West syndrome (WS), selected from a series of 103 WS patients, with a follow-up between 4 and 12 years, were studied retrospectively to verify whether this group included patients who fulfilled the criteria for an idiopathic etiology. WebApr 9, 2024 · Children suffering from symptomatic and cryptogenic West’s syndrome have a poor prognosis especially if they do not respond to treatment. According to statistics, 5 in every 100 children having West’s … WebApproximately 30% of children with LGS have a history of other types of childhood epilepsy, including West syndrome, Ohtahara syndrome, and infantile spasms, which progress and evolve to LGS. 1,10. Etiology of Idiopathic (Cryptogenic) LGS. In approximately 25% of cases of LGS, no underlying pathological explanation can be identified. pantex dr couteel