Answers are grounded in this paper and cite their sources.
Update examines myopathies linked to underlying conditions, highlighting new treatments and autoimmune factors.
This update begins with a discussion of treatable lipid storage myopathies associated with the use of sertraline and ranolazine. We then turn to monoclonal gammopathy-associated myopathies including a more recently identified disorder that is also treatment-responsive, monoclonal gammopathy-associated glycogen storage myopathy. Several reports on statins and muscle symptoms, toxic myopathy, and immune-mediated necrotizing myopathy follow. Other autoimmune myopathy topics are highlighted. Then, muscular dystrophies are covered with a focus on dystrophinopathies, limb-girdle muscular dystrophy, and facioscapulohumeral muscular dystrophy. Pompe disease follows with a focus on enzyme replacement therapy data. A short section on congenital myopathies precedes a review of reports on myotonic dystrophies and nondystrophic myotonias.
No takes yet. Share an insight, caveat, or question.
Isfort et al. (2026) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: