Cargando…
MCT oil-based diet reverses hypertrophic cardiomyopathy in a patient with very long chain acyl-coA dehydrogenase deficiency
Very long chain acyl-CoA dehydrogenase (VLCAD) deficiency is one of the genetic defects of mitochondrial fatty acid beta-oxidation presenting in early infancy or childhood. If undiagnosed and untreated, VLCAD deficiency may be fatal, secondary to cardiac involvement. We assessed the effect of replac...
Autores principales: | Pervaiz, Muhammad Ali, Kendal, Fran, Hegde, Madhuri, Singh, Rani H. |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3144685/ https://www.ncbi.nlm.nih.gov/pubmed/21814341 http://dx.doi.org/10.4103/0971-6866.82190 |
Ejemplares similares
-
Cardiac Hypertrophy in Mice with Long-Chain Acyl-CoA Dehydrogenase (LCAD) or Very Long-Chain Acyl-CoA Dehydrogenase (VLCAD) Deficiency
por: Cox, Keith B., et al.
Publicado: (2009) -
Medium-Chain Acyl-CoA Dehydrogenase Deficiency in an Infant with Dilated Cardiomyopathy
por: Marcì, Marcello, et al.
Publicado: (2009) -
Very-Long-Chain Acyl-CoA Dehydrogenase Deficiency: Family Impact and Perspectives
por: Crawford, Sarah, et al.
Publicado: (2023) -
Rhabdomyolysis in a neonate due to very long chain acyl CoA dehydrogenase deficiency
por: Scott Schwoerer, Jessica, et al.
Publicado: (2015) -
H(2)O(2) release from the very long chain acyl-CoA dehydrogenase
por: Kakimoto, Pâmela A.H.B., et al.
Publicado: (2015)