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Childhood onset nemaline myopathy, or mild nemaline myopathy is a type of nemaline myopathy (NM) characterized by distal muscle weakness, and sometimes slowness of muscle contraction.
Estimated prevalence: <1 in 1,000,000 (VERY_RARE).
No clinical trials have been registered for childhood-onset nemaline myopathy.
2 publications have been identified in PubMed for childhood-onset nemaline myopathy. Research spans Case Report / Case Series (50%) and Epidemiology / Natural History (50%).
Safi F (2025). [PMID: 39812211](https://pubmed.ncbi.nlm.nih.gov/39812211/). *La Tunisie medicale*. [Case Report / Case Series]
Hildebrandt C (2025). [PMID: 40661861](https://pubmed.ncbi.nlm.nih.gov/40661861/). *Neurology. Genetics*. [Epidemiology / Natural History]
Data assembled from 3 of 12 sources · Last updated Sep 20, 2026, 1:33 PM UTC
European rare disease database
Genetic and Rare Diseases Info Center