Progressive neuropathy and recurrent myoglobinuria in a child with long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency
- 31 May 1991
- journal article
- case report
- Published by Elsevier in The Journal of Pediatrics
- Vol. 118 (5) , 744-746
- https://doi.org/10.1016/s0022-3476(05)80039-3
Abstract
No abstract availableThis publication has 5 references indexed in Scilit:
- SUDDEN INFANT DEATH AND LONG-CHAIN 3-HYDROXYACYL-CoA DEHYDROGENASEThe Lancet, 1989
- Abnormalities of Fatty Acid OxidationNew England Journal of Medicine, 1988
- Long-Chain Acyl-Coenzyme A Dehydrogenase Deficiency: Biochemical Studies in Fibroblasts from Three PatientsPediatric Research, 1988
- Long-Chain Acyl Coenzyme A Dehydrogenase Deficiency: An Inherited Cause of Nonketotic HypoglycemiaPediatric Research, 1985
- Hypoglycemia, Hepatic Dysfunction, Muscle Weakness, Cardiomyopathy, Free Carnitine Deficiency and Long-Chain Acylcarnitine Excess Responsive to Medium Chain Triglyceride DietPediatric Research, 1983