Maladies musculaires de l’adulte : quand évoquer le diagnostic ? [Muscle disease in the adults: when to suspect it?]

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State: Public
Version: Final published version
License: CC BY-NC-ND 4.0
Serval ID
serval:BIB_3871D1A3BE8F
Type
Article: article from journal or magazin.
Publication sub-type
Review (review): journal as complete as possible of one specific subject, written based on exhaustive analyses from published work.
Collection
Publications
Institution
Title
Maladies musculaires de l’adulte : quand évoquer le diagnostic ? [Muscle disease in the adults: when to suspect it?]
Journal
Revue medicale suisse
Author(s)
Vicino A., Fayolle D., Ochsner F., Echaniz-Laguna A., Magy L., Hübers A., Théaudin M.
ISSN
1660-9379 (Print)
ISSN-L
1660-9379
Publication state
Published
Issued date
27/04/2022
Peer-reviewed
Oui
Volume
18
Number
779
Pages
799-802
Language
french
Notes
Publication types: Journal Article
Publication Status: ppublish
Abstract
Muscle diseases or myopathies have heterogeneous clinical presentations and etiologies. The principal sign is muscular weakness, whose distribution can help diagnostic orientation. Exercise intolerance, even without weakness at rest, can indicate an underlying myopathy. An isolated CK elevation can have multiple causes, but its persistence after a period of rest can point towards a subclinical myopathy. Isolated myalgia, especially at rest, are usually not associated with muscle disease. If the suspicion of myopathy is high, the patient will be assessed by a neurologist trained in muscle disorders, with correlation of clinical and neurophysiological findings, muscle imaging and, if indicated, muscle biopsy and genetic analysis. Cardiac and respiratory assessments are mandatory if a myopathy is suspected.
Keywords
Adult, Biopsy, Heart, Humans, Muscles, Muscular Diseases/diagnosis, Muscular Diseases/etiology, Myalgia/complications
Pubmed
Create date
16/05/2022 10:55
Last modification date
17/08/2022 7:09
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