Seizure outcome in infantile spasms-A retrospective study

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A retrospective study on aetiology based outcome of infantile spasms

PURPOSE The goal of this retrospective study is to review the causes of infantile spasms and to correlate aetiology with outcome. METHODS All children diagnosed with infantile spasms between 1990 and 2003 at our institution were included. Charts were reviewed for the presence or absence of a defined aetiology/association, response to treatment, long-term epileptic and cognitive outcome. RES...

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Outcome of patients with infantile spasms.

PURPOSE To assess outcome of children diagnosed with infantile spasms (IS) during the six-year-period (2002-20006), at the Pediatric Clinic of Clinical Center of University of Sarajevo, as well as to present other important clinical characteristics in this group of patients. METHODS All patients had medical histories with detailed description orvideo recordings of their seizures, as well as p...

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West's Syndrome (infantile Spasms)--a Polymyographic Study.

A syndrome of brief repetitive massive spasms involving the muscles of the neck, trunk, and limbs, accompanied by either regression or loss of motor and mental skills, was described by Dr. W. J. West, a practitioner in Tonbridge, in his own son (1841). Dr. West had taken the child to London for a consultation with Sir Charles Clarke who had already seen four cases of what he called the 'salaam ...

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Infantile spasms.

Infantile spasms constitute both a distinctive seizure type and an age-specific epilepsy syndrome that have been extensively described for over a century. Standardization of the classification of infantile spasms has evolved, culminating in recent recommendations for separately recognizing and distinguishing the seizure type (spasms or epileptic spasms) and the epilepsy syndrome of infantile sp...

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Infantile spasms.

Overview Infantile spasms, also known as West syndrome, is a catastrophic childhood epilepsy with seizures that are difficult to control; it is associated with mental retardation. It usually has an onset during the first year of life, and typically between 4 and 8 months. Early recognition, careful diagnostic evaluation, and proper treatment may allow some children to attain seizure control and...

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ژورنال

عنوان ژورنال: Epilepsia

سال: 2011

ISSN: 0013-9580

DOI: 10.1111/j.1528-1167.2010.02963.x