منابع مشابه
Differential diagnosis and evaluation in pediatric inflammatory demyelinating disorders.
Major advances have been made in the clinical and radiologic characterization of children presenting with the different forms of an acquired inflammatory demyelinating syndrome (ADS) such as acute disseminating encephalomyelitis, neuromyelitis optica spectrum disorders, and clinically isolated syndromes. Nevertheless, a proportion of cases that present with similar symptoms are due to a broad s...
متن کاملDemyelinating Disorders
as in men and more frequently afflicts Caucasian patients, but all races can be affected. Onset of disease usually occurs in people between 20 and 50 years of age, with a peak occurring in those 30 years of age. The prevalence of MS varies widely with location; the highest prevalence is found at higher latitudes. This geographic variation suggests that MS may in part be caused by the action of ...
متن کاملConsensus definitions for pediatric MS and other demyelinating disorders in childhood.
In light of the published 2012 International Pediatric Multiple Sclerosis Group definitions for pediatric multiple sclerosis (MS) and related disorders and given that pediatric-onset MS is now formally included in the 2010 McDonald criteria for MS, we sought to review these criteria and summarize their application in children with acquired CNS demyelination. In addition, proposals are made for ...
متن کاملPediatric demyelinating diseases: multiple sclerosis or not?
tral nervous system demyelination have been increasingly recognized in children. Moreover, a much higher proportion of children (as compared to adults) suffer from a monophasic (and not chronic) demyelinating event such as acute disseminated encephalomyelitis or isolated optic neuritis, and transverse myelitis, often post-infectious. Differentiation between such acute monophasic illnesses and a...
متن کاملChronic Inflammatory Demyelinating Polyradiculoneuropathy and Related Disorders
The first case of recurrent neuritis was published by Eichhorst in 1890 (1). In 1958, Austin (2) described steroid responsiveness, recurrence and cerebrospinal fluid (CSF) protein elevation. Dyck and colleagues (3) described the clinicopathological findings of monophasic progression, steady deterioration, stepwise progression and recurrence, with histologic peripheral nervious system (PNS) infl...
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ژورنال
عنوان ژورنال: Neurology
سال: 2016
ISSN: 0028-3878,1526-632X
DOI: 10.1212/wnl.0000000000002882