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Typical nemaline myopathy is a moderate neonatal form of nemaline myopathy (NM) characterized by facial and skeletal muscle weakness and mild respiratory involvement.
Estimated prevalence: 1-9 in 100,000 (Uncommon).
No clinical trials have been registered for typical nemaline myopathy.
5 publications have been identified in PubMed for typical nemaline myopathy. Research spans Basic Science / Preclinical (40%), Epidemiology / Natural History (40%), and Case Report / Case Series (20%).
Safi F (2025). [PMID: 39812211](https://pubmed.ncbi.nlm.nih.gov/39812211/). *La Tunisie medicale*. [Case Report / Case Series]
Dofash LNH (2025). [PMID: 40581737](https://pubmed.ncbi.nlm.nih.gov/40581737/). *Human molecular genetics*. [Basic Science / Preclinical]
Hildebrandt C (2025). [PMID: 40661861](https://pubmed.ncbi.nlm.nih.gov/40661861/). *Neurology. Genetics*. [Epidemiology / Natural History]
van Kleef ESB (2024). [PMID: 39180840](https://pubmed.ncbi.nlm.nih.gov/39180840/). *Neuromuscular disorders : NMD*. [Epidemiology / Natural History]
Wang Y (2024). [PMID: 38733812](https://pubmed.ncbi.nlm.nih.gov/38733812/). *Stem cell research*. [Basic Science / Preclinical]
Data assembled from 3 of 12 sources · Last updated Sep 18, 2026, 7:32 PM UTC
European rare disease database
Genetic and Rare Diseases Info Center