Cargando…
New Acylcarnitine Ratio as a Reliable Indicator of Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency
Long-chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) and mitochondrial trifunctional protein (MTP) deficiencies are rare fatal disorders of fatty acid β-oxidation with no apparent genotype–phenotype correlation. The measurement of acylcarnitines by MS/MS is a current diagnostic workup in these disorde...
Autores principales: | Baydakova, Galina V., Tsygankova, Polina G., Pechatnikova, Natalia L., Bazhanova, Olga A., Nazarenko, Yana D., Zakharova, Ekaterina Y. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10531771/ https://www.ncbi.nlm.nih.gov/pubmed/37754774 http://dx.doi.org/10.3390/ijns9030048 |
Ejemplares similares
-
Management of pregnancy in a patient with long‐chain 3‐hydroxyacyl CoA dehydrogenase deficiency
por: Shakerdi, Loai A., et al.
Publicado: (2022) -
The Hypoglycemic Phenotype Is Islet Cell–Autonomous in Short-Chain Hydroxyacyl-CoA Dehydrogenase–Deficient Mice
por: Molven, Anders, et al.
Publicado: (2016) -
Newborn Screening for Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase and Mitochondrial Trifunctional Protein Deficiencies Using Acylcarnitines Measurement in Dried Blood Spots—A Systematic Review of Test Accuracy
por: Stinton, Chris, et al.
Publicado: (2021) -
Leptospiral 3-hydroxyacyl-CoA dehydrogenase as an early urinary biomarker of leptospirosis
por: Toma, Claudia, et al.
Publicado: (2018) -
Enoyl-CoA hydratase/3-hydroxyacyl CoA dehydrogenase is essential for the production of DHA in zebrafish
por: Yang, Gang, et al.
Publicado: (2022)