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Adult-onset nemaline myopathy is a rapidly progressive type of nemaline myopathy (NM) characterized by a very late onset.
Estimated prevalence: <1 in 1,000,000 (VERY_RARE).
No clinical trials have been registered for adult-onset nemaline myopathy.
4 publications have been identified in PubMed for adult-onset nemaline myopathy. Research spans Case Report / Case Series (75%) and Review / Meta-Analysis (25%).
Torchia E (2026). [PMID: 41483665](https://pubmed.ncbi.nlm.nih.gov/41483665/). *Neuromuscul Disord*. [Case Report / Case Series]
Miyata A (2025). [PMID: 40540855](https://pubmed.ncbi.nlm.nih.gov/40540855/). *Neuromuscul Disord*. [Review / Meta-Analysis]
Narwal A (2024). [PMID: 39691005](https://pubmed.ncbi.nlm.nih.gov/39691005/). *Neurol India*. [Case Report / Case Series]
Dalal N (2024). [PMID: 38866581](https://pubmed.ncbi.nlm.nih.gov/38866581/). *BMJ Case Rep*. [Case Report / Case Series]
Data assembled from 3 of 12 sources · Last updated Sep 20, 2026, 6:24 PM UTC
European rare disease database
Genetic and Rare Diseases Info Center
Common questions about adult-onset nemaline myopathy