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No clinical trials have been registered for multiple acyl-CoA dehydrogenase deficiency, mild type.
6 publications have been identified in PubMed for multiple acyl-CoA dehydrogenase deficiency, mild type. Research spans Case Report / Case Series (50%), Review / Meta-Analysis (33%), and Epidemiology / Natural History (17%).
Jaeger B (2026). [PMID: 42046426](https://pubmed.ncbi.nlm.nih.gov/42046426/). *J Inherit Metab Dis*. [Review / Meta-Analysis]
Barbetti R (2026). [PMID: 42181774](https://pubmed.ncbi.nlm.nih.gov/42181774/). *Mol Genet Metab Rep*. [Case Report / Case Series]
Upadia J (2025). [PMID: 41440808](https://pubmed.ncbi.nlm.nih.gov/41440808/). *International journal of neonatal screening*. [Epidemiology / Natural History]
Parvini F (2025). [PMID: 41254678](https://pubmed.ncbi.nlm.nih.gov/41254678/). *Orphanet journal of rare diseases*. [Case Report / Case Series]
Seyedtaghia MR (2024). [PMID: 38967380](https://pubmed.ncbi.nlm.nih.gov/38967380/). *Molecular genetics & genomic medicine*. [Review / Meta-Analysis]
Data assembled from 3 of 12 sources · Last updated Sep 20, 2026, 11:09 AM UTC
European rare disease database
Genetic and Rare Diseases Info Center
Ingoglia F (2024). [PMID: 39318848](https://pubmed.ncbi.nlm.nih.gov/39318848/). *Molecular genetics and metabolism reports*. [Case Report / Case Series]