Patterns and severity of conduction abnormalities in Guillain-Barré syndrome
- PMID: 1659615
- PMCID: PMC1014513
- DOI: 10.1136/jnnp.54.9.768
Patterns and severity of conduction abnormalities in Guillain-Barré syndrome
Abstract
Whether the conduction abnormalities and lesions underlying them are randomly distributed throughout the peripheral nervous system (PNS) or certain regions are selectively more vulnerable to attack is an unresolved question in Guillain-Barré syndrome (GBS). To examine this question, 15 cases of GBS were comprehensively examined using electrophysiological techniques which allowed close examination, quantitation and comparison of conduction abnormalities in motor and sensory fibres of the upper limb between the spinal cord and the distal extremities of the nerve fibres. Comparison of these studies with results expected in a model where the chances of conduction failure were uniformly distributed led to the conclusion that conduction slowing and block were not uniformly distributed in most cases. Conduction block was maximal in the terminal segment distal to the wrist and to a lesser extent both conduction block and conduction slowing were disproportionately greater across the elbow and in the axillary to spinal root segments in over one half of the cases. These findings support the hypothesis that certain regions, perhaps because of relative deficiencies of the blood-nerve barrier, may be more vulnerable in GBS than other regions.
Similar articles
-
[Value of magnetic stimulation and F-wave determination in diagnosis of proximal demyelinating lesions. Follow-up of acute Guillain-Barré polyradiculitis].Nervenarzt. 1998 Apr;69(4):338-41. doi: 10.1007/s001150050280. Nervenarzt. 1998. PMID: 9606686 German.
-
Guillain-Barré syndrome: a model of random conduction block.J Neurol Neurosurg Psychiatry. 1988 Sep;51(9):1158-63. doi: 10.1136/jnnp.51.9.1158. J Neurol Neurosurg Psychiatry. 1988. PMID: 3225598 Free PMC article.
-
Sequence of demyelination-remyelination in Guillain-Barré disease.J Neurol Neurosurg Psychiatry. 1983 Feb;46(2):168-74. doi: 10.1136/jnnp.46.2.168. J Neurol Neurosurg Psychiatry. 1983. PMID: 6842222 Free PMC article.
-
[Physiological approach to peripheral neuropathy. Conventional nerve conduction studies and magnetic motor root stimulation].Rinsho Shinkeigaku. 2004 Nov;44(11):986-90. Rinsho Shinkeigaku. 2004. PMID: 15651350 Review. Japanese.
-
Guillain-Barré syndrome: clinical neurophysiologic studies.Rev Neurol (Paris). 1996 May;152(5):339-43. Rev Neurol (Paris). 1996. PMID: 8881426 Review.
Cited by
-
The sural-sparing pattern in clinical variants and electrophysiological subtypes of Guillain-Barré syndrome.Arq Neuropsiquiatr. 2024 Apr;82(4):1-7. doi: 10.1055/s-0044-1785692. Epub 2024 Apr 19. Arq Neuropsiquiatr. 2024. PMID: 38641340 Free PMC article.
-
Distribution patterns of demyelination correlate with clinical profiles in chronic inflammatory demyelinating polyneuropathy.J Neurol Neurosurg Psychiatry. 2002 Jan;72(1):37-42. doi: 10.1136/jnnp.72.1.37. J Neurol Neurosurg Psychiatry. 2002. PMID: 11784822 Free PMC article.
-
Clinical Characteristics of Intravenous Injection of Monosialotetrahexosyl Ganglioside Sodium-Related Guillain-Barre Syndrome.Front Neurol. 2019 Mar 15;10:225. doi: 10.3389/fneur.2019.00225. eCollection 2019. Front Neurol. 2019. PMID: 30930839 Free PMC article.
-
Voluntary contraction impairs the refractory period of transmission in healthy human axons.J Physiol. 2001 Feb 15;531(Pt 1):265-75. doi: 10.1111/j.1469-7793.2001.0265j.x. J Physiol. 2001. PMID: 11179409 Free PMC article.
-
Electrophysiological sequels of inflammatory demyelination.J Neurol Neurosurg Psychiatry. 1994 Nov;57 Suppl(Suppl):29-32. doi: 10.1136/jnnp.57.suppl.29. J Neurol Neurosurg Psychiatry. 1994. PMID: 7964848 Free PMC article. Review. No abstract available.
References
MeSH terms
LinkOut - more resources
Full Text Sources