Abstract
Heart muscle from infants who died unexpectedly and who showed fatty changes in the liver at necropsy was analysed for long chain and medium chain acylcoenzyme A dehydrogenase activities by using the natural electron acceptor. In two of the seven cases investigated a deficiency in acylcoenzyme A dehydrogenase activity was found. In one case the deficiency was in medium chain acylcoenzyme A dehydrogenase activity and in the other long chain acylcoenzyme A dehydrogenase activity.
These findings emphasise the importance of investigating fatty acid oxidation in infants who have died unexpectedly.
Full text
PDFSelected References
These references are in PubMed. This may not be the complete list of references from this article.
- Coates P. M., Hale D. E., Stanley C. A., Corkey B. E., Cortner J. A. Genetic deficiency of medium-chain acyl coenzyme A dehydrogenase: studies in cultured skin fibroblasts and peripheral mononuclear leukocytes. Pediatr Res. 1985 Jul;19(7):671–676. doi: 10.1203/00006450-198507000-00007. [DOI] [PubMed] [Google Scholar]
- LOWRY O. H., ROSEBROUGH N. J., FARR A. L., RANDALL R. J. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951 Nov;193(1):265–275. [PubMed] [Google Scholar]
- Mooy P. D., Przyrembel H., Giesberts M. A., Scholte H. R., Blom W., van Gelderen H. H. Glutaric aciduria type II: treatment with riboflavine, carnitine and insulin. Eur J Pediatr. 1984 Dec;143(2):92–95. doi: 10.1007/BF00445792. [DOI] [PubMed] [Google Scholar]
- Pollitt R. J. Inherited disorders of straight chain fatty acid oxidation. Arch Dis Child. 1987 Jan;62(1):6–7. doi: 10.1136/adc.62.1.6. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sudden infant death and inherited disorders of fat oxidation. Lancet. 1986 Nov 8;2(8515):1073–1075. [PubMed] [Google Scholar]