Guillain-Barré syndrome diagnostic study of choice: Difference between revisions
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Created page with "__NOTOC__ {{Guillain-Barré syndrome}} {{CMG}}; {{AE}} {{Fs}} == Overview == == Diagnostic Study of Choice == === Study of choice === [Name of the investigation] is the gold..." |
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== Diagnostic Study of Choice == | == Diagnostic Study of Choice == | ||
=== | === Diagnostic Criteria === | ||
* There is no single diagnostic study of choice for Guillain Barre syndrome, though GBS may be diagnosed based on NINDS criteria established by National Institute of Neurological Disorders and Stroke:<ref name="pmid2194422">{{cite journal |vauthors=Asbury AK, Cornblath DR |title=Assessment of current diagnostic criteria for Guillain-Barré syndrome |journal=Ann. Neurol. |volume=27 Suppl |issue= |pages=S21–4 |date=1990 |pmid=2194422 |doi= |url=}}</ref> | |||
** Progressive ascending weakness or paralysis usually starting from legs, involving are 4 limbs, the trunk, bulbar and facial muscles, and external ocular muscles. | |||
** Areflexia or decreased reflexes in affected limbs. | |||
* these findings can make the GBS diagnosis even more possible: | |||
** Progression of symptoms over days to four weeks | |||
** Relative symmetry | |||
** Sensory abnormalities | |||
** Cranial nerve involvement, especially bilateral facial nerve weakness | |||
** Recovery starting two to four weeks after progression stops | |||
** Autonomic disturbance | |||
** Pain | |||
* | ** absence of fever in the acute phase | ||
** Elevated CSF protein level | |||
** CSF cell count ≤50/mm<sup>3</sup> | |||
** Electrodiagnostic abnormalities consistent with GBS | |||
There is no single diagnostic study of choice for | |||
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==References== | ==References== |
Revision as of 18:49, 18 December 2018
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Fahimeh Shojaei, M.D.
Overview
Diagnostic Study of Choice
Diagnostic Criteria
- There is no single diagnostic study of choice for Guillain Barre syndrome, though GBS may be diagnosed based on NINDS criteria established by National Institute of Neurological Disorders and Stroke:[1]
- Progressive ascending weakness or paralysis usually starting from legs, involving are 4 limbs, the trunk, bulbar and facial muscles, and external ocular muscles.
- Areflexia or decreased reflexes in affected limbs.
- these findings can make the GBS diagnosis even more possible:
- Progression of symptoms over days to four weeks
- Relative symmetry
- Sensory abnormalities
- Cranial nerve involvement, especially bilateral facial nerve weakness
- Recovery starting two to four weeks after progression stops
- Autonomic disturbance
- Pain
- absence of fever in the acute phase
- Elevated CSF protein level
- CSF cell count ≤50/mm3
- Electrodiagnostic abnormalities consistent with GBS