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A group of myopathies that includes Emery-Dreifuss muscular dystrophy (EDMD), and two allelic disorders characterized by the presence of reducing body on histopathology, namely reducing body myopathy (RBM) and scapuloperoneal myopathy.
No clinical trials have been registered for FHL1-related myopathy.
7 publications have been identified in PubMed for FHL1-related myopathy. Research spans Case Report / Case Series (86%) and Basic Science / Preclinical (14%).
Lv X (2026). [PMID: 41021222](https://pubmed.ncbi.nlm.nih.gov/41021222/). *JAMA neurology*. [Case Report / Case Series]
Zhang H (2026). [PMID: 41839840](https://pubmed.ncbi.nlm.nih.gov/41839840/). *The Journal of international medical research*. [Case Report / Case Series]
Severa G (2026). [PMID: 42256499](https://pubmed.ncbi.nlm.nih.gov/42256499/). *Neurol Genet*. [Case Report / Case Series]
Shimazaki R (2025). [PMID: 41254906](https://pubmed.ncbi.nlm.nih.gov/41254906/). *Annals of clinical and translational neurology*. [Basic Science / Preclinical]
Gowda VK (2025). [PMID: 41188006](https://pubmed.ncbi.nlm.nih.gov/41188006/). *BMJ case reports*. [Case Report / Case Series]
Data assembled from 2 of 12 sources · Last updated Sep 18, 2026, 11:35 PM UTC
Common questions about FHL1-related myopathy
Zhang S (2025). [PMID: 41368035](https://pubmed.ncbi.nlm.nih.gov/41368035/). *BMJ neurology open*. [Case Report / Case Series]