Recognizing Myopathy in Patients with Muscle Weakness or Pain.


Journal

Primary care
ISSN: 1558-299X
Titre abrégé: Prim Care
Pays: United States
ID NLM: 0430463

Informations de publication

Date de publication:
Jun 2024
Historique:
medline: 2 5 2024
pubmed: 2 5 2024
entrez: 1 5 2024
Statut: ppublish

Résumé

Muscle weakness and pain can be seen in orthopedic, rheumatologic, cardiac, and musculoskeletal conditions in addition to neurologic disorders. Myopathy, which describes a heterogenous group of hereditary and acquired disorders that affect muscle channels, structure, and metabolism, is one possible cause. This review focuses on essential information to support primary care providers as they assess patients with muscle weakness and pain for myopathy. As with most neurologic disorders, a thorough clinical history and physical examination are essential first steps. These findings will then guide diagnostic testing and facilitate appropriate management or referral for further neuromuscular care.

Identifiants

pubmed: 38692777
pii: S0095-4543(24)00007-1
doi: 10.1016/j.pop.2024.02.005
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

311-326

Informations de copyright

Copyright © 2024 Elsevier Inc. All rights reserved.

Déclaration de conflit d'intérêts

Disclosure M.A. Elafros acknowledges funding from NIH, United States NINDS K23NS131444 and the Andrea and Lawrence A. Wolfe Research Professorship. A. Seth has served as a consultant for Argenx, UCB, and Takeda Pharmaceuticals.

Auteurs

Melissa A Elafros (MA)

Department of Neurology, University of Michigan, 5015 AAT-BSRB, 109 Zina Pitcher Place, Ann Arbor, MI 48109, USA. Electronic address: elafrome@med.umich.edu.

Arjun Seth (A)

Department of Neurology, Northwestern University, 710 North Lake Shore Drive, Abbott Hall, 11th floor, Office #1112, Chicago, IL 60611, USA.

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Classifications MeSH