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Puslapis 1 nuo 831 rezultatus
Partial seizures in West syndrome.
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OBJECTIVE
To study the occurrence of partial seizures (PS) and elucidate the characteristics of patients with West syndrome (WS) with PS.
METHODS
We investigated the electroclinical and radiologic features in 92 children with WS who were older than 3 years at follow-up.
RESULTS
Thirty-six (39.1%)
Outcome in West syndrome.
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OBJECTIVE
To assess the seizure and developmental outcome in children with West syndrome with respect to treatment lag.
METHODS
Twenty-six children satisfying inclusion criteria of West syndrome i.e., infantile spasms, psychomotor retardation and abnormal EEG pattern were prospectively evaluated.
Familial idiopathic West syndrome.
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Two families, each with occurrence of West syndrome in two siblings, are presented. Monozygotic twins in family 1 developed infantile spasms at the age of 4 months. Two female siblings in family 2 started to have seizures at the age of 6 months, but 2 years apart. The family history; development
DMD and West syndrome.
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Duchenne Muscular Dystrophy (DMD) is the most frequent muscular dystrophy in childhood, with a worldwide incidence of one in 5000 live male births. It is due to mutations in the dystrophin gene leading to absence of full-length dystrophin protein. Central nervous system involvement is well-known in
What is West syndrome?
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The combination of axial spasms in clusters, hypsarrhythmia, and psychomotor delay beginning in the first year of life defines West syndrome. Variants of this classical triad comprise variations of age of onset ranging from the first month to 4 years, spasms that may be asymmetrical or combined with
[West Nile virus (WNV) encephalitis].
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A DISEASE ON THE COME BACK: West Nile encephalitis has been known since the thirties. It generally occurs in Africa and Western Asia, rarely in Europe. The disease has disappeared from France since 1960, but has reappeared in the United States and in Israel. A SEVERE VIRAL INFECTION: West Nile
Induced microseizures in West syndrome.
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Induced microseizures (IMS) were observed in a 5-month-old girl with symptomatic West syndrome. The seizures occurred following the suppression of infantile spasms with adrenocorticotropic hormone therapy and disappeared following the cessation of clonazepam administration. The ictal manifestations
West syndrome associated with porencephaly.
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A 3-year-old boy with West syndrome who was shown to have a cystic lesion on magnetic resonance imagings underwent surgical treatment. He had been initially managed with several antiepileptic drugs, but abnormalities on electroencephalography (EEG) persisted. Histological examination of the cystic
[West syndrome in tuberous sclerosis].
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Observation's analysis of 5 children in age from 9 months to 4 years 11 months with tuberous sclerosis was performed. The initial manifestations of disease were following: early children form of epilepsy exactly infantile spasms (West syndrome) appearance, dermal alterations in the form of
West syndrome: individualized ACTH therapy.
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Individualized ACTH treatment of the West syndrome (WS) was assessed in a prospective multicenter study, in which each patient's dosage was increased stepwise according to response. Our series included six patients with cryptogenic and 24 with symptomatic infantile spasms. During the treatment
Surgical treatment of West syndrome.
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The discovery of focal or multifocal cortical lesions using magnetic resonance imaging (MRI) and positron emission tomography (PET) scanning in the majority of infants with West syndrome has led to a surgical approach in the treatment of some patients with intractable infantile spasms. The locations
Brain connectivity in West syndrome.
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OBJECTIVE
Hypsarrhythmia, the pathognomonic EEG pattern of West syndrome, is typically characterized by a high amplitude, arrhythmic, and asynchronous pattern. While this severely aberrant pattern would suggest severe abnormalities in connectivity, coherence has not yet been systematically assessed
West syndrome: the Philippine experience.
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OBJECTIVE
To provide information on the current status of West syndrome (WS) in the Philippines.
METHODS
This is a retrospective review of WS cases from January 1997 to December 1999 from two largest referral government institutions. A questionnaire interview survey on anticonvulsant usage was also
Unusual Cause of West Syndrome.
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Schimmelpenning-Feuerstein-Mims syndrome is a congenital neurocutaneous disorder, comprising of organoid epidermal nevus with a broad spectrum of multiorgan dysfunction (neurologic, skeletal, cardiovascular, ophthalmic, and urologic) secondary to postzygotic mutation in the early embryonic period.
[West syndrome: a chronobiological approach].
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OBJECTIVE
Chronobiology is the discipline involving the study of the time structure of living creatures. Since it has been shown that there is non-chaotic recurrence, at precise intervals of time, of different functions from unicellular level to complex human systems, rhythmometric evaluation of key
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