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Acute flaccid paralysis

Authors: Raposo Anna Julia Lacerda; Freire Eduardo Galvão; Ferreira, De Farias Célia Raiany; Serquiz E Pinheiro Renato; Pinheiro Francisco Irochima; Guzen Fausto Pierdoná; Rêgo Amália Cinhtia Meneses; +1 Authors

Acute flaccid paralysis

Abstract

Acute Flaccid Paralysis (AFP) is a syndrome characterized by a diffuse, acute muscular weakness that develops with hypotonia and deep or abolished hypoactive reflexes. Literature review of the last five years in the databases Pubmed, Scopus, Embase, and Web of Science. Data were collected from epidemiological studies using the keywords. AFP includes heterogeneous diseases, variable clinical presentation, and correlated with a specific etiology. The differential diagnosis of acute flaccid paralysis includes spinal cord diseases, acute polyneuropathies, myoneural plaque dysfunction, and muscle disease. PFAs represents a set of disorders used by the World Health Organization (WHO) as an indicator of polio eradication. Therefore, the knowledge and understanding of the respective etiologies are necessary to make their differential diagnosis and appropriate treatment.

Keywords

Paralysis; Acute inflammatory polyneuropathy; Acute autoimunne neuropathies; Acute infectious polyneuritis; Acute transverse myelitis; Myasthenic syndromes

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selected citations
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This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
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popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
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