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Reducing body myopathy (RBM) is a rare muscle disorder marked by progressive muscle weakness and the presence of characteristic inclusion bodies in affected muscle fibers.
Estimated prevalence: <1 in 1,000,000 (VERY_RARE).
No clinical trials have been registered for reducing body myopathy.
8 publications have been identified in PubMed for reducing body myopathy. Research spans Case Report / Case Series (50%), Basic Science / Preclinical (25%), and Review / Meta-Analysis (13%).
Severa G (2026). [PMID: 42256499](https://pubmed.ncbi.nlm.nih.gov/42256499/). *Neurol Genet*. [Case Report / Case Series]
Nagaraj CB (2025). [PMID: 40009419](https://pubmed.ncbi.nlm.nih.gov/40009419/). *Journal of clinical neuromuscular disease*. [Basic Science / Preclinical]
Finch M (2025). [PMID: 40388931](https://pubmed.ncbi.nlm.nih.gov/40388931/). *Journal of child neurology*. [Case Report / Case Series]
Zhang S (2025). [PMID: 41368035](https://pubmed.ncbi.nlm.nih.gov/41368035/). *BMJ neurology open*. [Clinical Trial Publication]
Gowda VK (2025). [PMID: 41188006](https://pubmed.ncbi.nlm.nih.gov/41188006/). *BMJ case reports*. [Case Report / Case Series]
Data assembled from 3 of 12 sources · Last updated Sep 18, 2026, 11:33 PM UTC
European rare disease database
Genetic and Rare Diseases Info Center
Caputo M (2024). [PMID: 40017287](https://pubmed.ncbi.nlm.nih.gov/40017287/). *Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology*. [Review / Meta-Analysis]
Aihara Y (2024). [PMID: 38933611](https://pubmed.ncbi.nlm.nih.gov/38933611/). *Cureus*. [Case Report / Case Series]