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Biochemical and molecular characteristics among infants with abnormal newborn screen for very-long-chain acyl-CoA dehydrogenase deficiency: A single center experience
OBJECTIVE: To define the biochemical and molecular characteristics and diagnostic outcomes of a large US cohort of VLCAD deficiency positive cases as detected by newborn screening (NBS) with MS:MS. This relatively common disorder of fatty acid oxidation is screened for in every state in America and...
Autores principales: | Upadia, Jariya, Noh, Grace, Lefante, John J., Andersson, Hans C. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10475501/ https://www.ncbi.nlm.nih.gov/pubmed/37671074 http://dx.doi.org/10.1016/j.ymgmr.2023.101002 |
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