Walsh & Hoyt: Pathogenesis and Pathophysiology

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Identifier wh_ch61_p3529
Title Walsh & Hoyt: Pathogenesis and Pathophysiology
Creator David I. Kaufman, DO
Affiliation Chair, Neurology & Ophthalmology, Michigan State University
Subject Demyelinating Diseases; Axonal Disorders; Acute Inflammatory Demyelinating Polyneuropathy; Pathogenesis; Pathophysiology
Description The pathologic findings in AIDP are consistent with an acquired immune-mediated disorder. Clinical immunologic studies and findings in an almost identical animal model called experimental allergic neuritis indicate that both humoral and cell-mediated systems may participate in production of the disease. AIDP may be caused by antibodies to nerve tissue or soluble immune complexes. Macrophages seem to be the chief effector cells mediating damage to myelin, apparently acting as antigen-presenting cells. There also is evidence of activation of T-lymphocytes, but it is unclear if these cells have a primary pathogenic function or simply are involved secondarily in the inflammatory process.
Date 2005
Language eng
Format application/pdf
Type Text
Source Walsh and Hoyt's Clinical Neuro-Ophthalmology, 6th Edition
Relation is Part of Walsh and Hoyt's Clinical Neuro-Ophthalmology Walsh and Hoyt's Clinical Neuro-Ophthalmology
Collection Neuro-ophthalmology Virtual Education Library: NOVEL http://NOVEL.utah.edu
Publisher Wolters Kluwer Health, Philadelphia
Holding Institution Spencer S. Eccles Health Sciences Library, University of Utah, 10 N 1900 E SLC, UT 84112-5890
Rights Management Copyright 2005. For further information regarding the rights to this collection, please visit: https://NOVEL.utah.edu/about/copyright
ARK ark:/87278/s6477k9w
Setname ehsl_novel_whts
ID 185735
Reference URL https://collections.lib.utah.edu/ark:/87278/s6477k9w
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