dc.contributor.author | ALzowai, Retaj Radi | |
dc.date.accessioned | 2020-07-07T10:05:01Z | |
dc.date.available | 2020-07-07T10:05:01Z | |
dc.date.issued | 2020-02-27 | |
dc.identifier.uri | http://repository.limu.edu.ly/handle/123456789/1710 | |
dc.description | Guillian Barre Syndrome GBS is rapidly progressive disorder of Muscle weakness
sometimes progressing to complete paralysis , this Syndrome effect approximately
only one or two people each year in every 100,000 population . Although its precise
cause is unknown . | en_US |
dc.description.abstract | Objective to report 2 cases of Guillian barre syndrome with different manifestations
Guillain Barre Syndrome consists of a group of neuropathic conditions characterized
by progressive weakness and diminished or absent mitotic reflexes.
The estimated annual incidence in the United States is 1.65 to 1.79 per 100,000
persons.
Guillain Barre syndrome is believed to result from an aberrant immune response that
attacks nerve tissue. This response may be triggered by surgery, immunizations, or
infections. The most common form of the disease, acute inflammatory demyelinating
polyradiculoneuropathy, presents as progressive motor weakness, usually beginning
in the legs and advancing proximally. Symptoms typically peak within four weeks,
then plateau before resolving.
More than one-half of patients experience severe pain, and about two-thirds have
autonomic symptoms, such as cardiac arrhythmias, blood pressure instability, or
urinary retention. Advancing symptoms may compromise respiration and vital
functions | en_US |
dc.language.iso | en | en_US |
dc.publisher | faculty of Basic Medical Science - Libyan International Medical University | en_US |
dc.rights | Attribution 3.0 United States | * |
dc.rights.uri | http://creativecommons.org/licenses/by/3.0/us/ | * |
dc.title | Guillain Barre Syndrome. | en_US |
dc.type | Other | en_US |