Sudden infant death syndrome and multiple acyl-coenzyme A dehydrogenase deficiency, ethylmalonic-adipic aciduria, or systemic carnitine deficiency
- 30 June 1987
- journal article
- research article
- Published by Elsevier BV in The Journal of Pediatrics
- Vol. 110 (6), 881-884
- https://doi.org/10.1016/s0022-3476(87)80401-8
Abstract
No abstract availableThis publication has 7 references indexed in Scilit:
- Recognition of medium-chain acyl-CoA dehydrogenase deficiency in asymptomatic siblings of children dying of sudden infant death or Reye-like syndromesThe Journal of Pediatrics, 1986
- Defects of metabolism of fatty acids in the sudden infant death syndrome.BMJ, 1985
- Riboflavin‐responsive ethylmalonic—adipic aciduriaJournal of Inherited Metabolic Disease, 1984
- Multiple acyl-CoA dehydrogenase deficiency occurring in pregnancy and caused by a defect in riboflavin metabolism in the mother: Study of a kindred with seven deaths in infancy: Value of riboflavin therapy in preventing this syndromeThe Journal of Pediatrics, 1983
- The analysis of plasma and urinary organic acids during prolonged fasting differentiates between systemic carnitine deficiency and a defect of fatty acid oxidationJournal of Inherited Metabolic Disease, 1983
- Systemic Carnitine Deficiency Presenting as Familial Endocardial FibroelastosisNew England Journal of Medicine, 1981
- Ethylmalonic-Adipic AciduriaJCI Insight, 1979