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Biomarker and diagnostic research for multiple acyl-CoA dehydrogenase deficiency, severe neonatal type has been reported in the published literature.
No clinical trials have been registered for multiple acyl-CoA dehydrogenase deficiency, severe neonatal type.
4 publications have been identified in PubMed for multiple acyl-CoA dehydrogenase deficiency, severe neonatal type. Research spans Case Report / Case Series (75%) and Diagnostic / Biomarker (25%).
Upadia J (2025). [PMID: 41440808](https://pubmed.ncbi.nlm.nih.gov/41440808/). *Int J Neonatal Screen*. [Diagnostic / Biomarker]
Parvini F (2025). [PMID: 41254678](https://pubmed.ncbi.nlm.nih.gov/41254678/). *Orphanet J Rare Dis*. [Case Report / Case Series]
Zhang Y (2025). [PMID: 39963347](https://pubmed.ncbi.nlm.nih.gov/39963347/). *Front Pediatr*. [Case Report / Case Series]
Li XX (2024). [PMID: 39156098](https://pubmed.ncbi.nlm.nih.gov/39156098/). *World J Clin Cases*. [Case Report / Case Series]
Data assembled from 3 of 12 sources · Last updated Sep 18, 2026, 1:32 PM UTC
European rare disease database
Genetic and Rare Diseases Info Center