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Publication year
2007Author(s)
Source
Journal of Neurology, 254, 6, (2007), pp. 695-704ISSN
Publication type
Article / Letter to editor

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Organization
Neurology
Journal title
Journal of Neurology
Volume
vol. 254
Issue
iss. 6
Page start
p. 695
Page end
p. 704
Subject
DCN 2: Functional Neurogenomics; UMCN 3.1: Neuromuscular development and genetic disordersAbstract
Neuralgic amyotrophy is a distinct clinical syndrome with acute severe pain and patchy paresis in the shoulder and arm region. The clinical phenotype was recently found to be more comprehensive and the long-term prognosis less optimistic than usually assumed for many patients. The disorder can be idiopathic or hereditary in an autosomal dominant fashion, with only few phenotypical variations between the two. This article provides a practical overview of current knowledge on the clinical presentation, diagnosis, pathogenesis and the treatment of pain and complications.
This item appears in the following Collection(s)
- Academic publications [227900]
- Electronic publications [107393]
- Faculty of Medical Sciences [86236]
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