Recognizing Myopathy in Patients with Muscle Weakness or Pain.
Acquired
Hereditary
Inflammatory
Muscular dystrophy
Myotonic dystrophy
Journal
Primary care
ISSN: 1558-299X
Titre abrégé: Prim Care
Pays: United States
ID NLM: 0430463
Informations de publication
Date de publication:
Jun 2024
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
311-326Informations 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.