PRENATAL DIAGNOSIS OF MEDIUM-CHAIN ACYL-CoA DEHYDROGENASE DEFICIENCY IN FAMILY WITH SUDDEN INFANT DEATH
- 21 February 1987
- journal article
- other
- Published by Elsevier in The Lancet
- Vol. 329 (8530), 440-441
- https://doi.org/10.1016/s0140-6736(87)90135-8
Abstract
No abstract availableThis publication has 6 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
- Genetic Deficiency of Medium-Chain Acyl Coenzyme A Dehydrogenase: Studies in Cultured Skin Fibroblasts and Peripheral Mononuclear LeukocytesPediatric Research, 1985
- Defects of metabolism of fatty acids in the sudden infant death syndrome.BMJ, 1985
- Fluorometric assay of acyl-CoA dehydrogenases in normal and mutant human fibroblastsBiochemical Medicine, 1985
- Deficiency of medium chain fatty acylcoenzyme A dehydrogenase presenting as the sudden infant death syndrome.BMJ, 1984
- Glutaric aciduria type II: Biochemical investigation and treatment of a child diagnosed prenatallyJournal of Inherited Metabolic Disease, 1983