Fatal outcome in a patient with long‐chain 3‐hydroxyacyl‐CoA dehydrogenase deficiency
- 1 March 1992
- journal article
- case report
- Published by Wiley in Journal of Inherited Metabolic Disease
- Vol. 15 (2), 278-279
- https://doi.org/10.1007/bf01799642
Abstract
No abstract availableThis publication has 3 references indexed in Scilit:
- 3-Hydroxydicarboxylic aciduria due to long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency associated with sudden neonatal death: protective effect of medium-chain triglyceride treatmentEuropean Journal of Pediatrics, 1991
- Prophylaxis of early ventricular fibrillation by inhibition of acylcarnitine accumulation.JCI Insight, 1989
- A new case of C6–C14 dicarboxylic aciduria with favourable evolutionJournal of Inherited Metabolic Disease, 1986