Heterozygosity for long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency and deterioration in liver function in a newborn infant infected with human immunodeficiency virus
- 31 October 1995
- journal article
- Published by Elsevier in The Journal of Pediatrics
- Vol. 127 (4) , 599-602
- https://doi.org/10.1016/s0022-3476(95)70122-2
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
- Secondary 3‐hydroxydicarboxylic aciduria mimicking long‐chain 3‐hydroxyacyl‐CoA dehydrogenase deficiencyJournal of Inherited Metabolic Disease, 1994
- Pregnancy and fetal long-chain 3-hydroxyacyl coenzyme A dehydrogenase deficiencyThe Lancet, 1993
- Human trifunctional protein deficiency: A new disorder of mitochondrial fatty acid β-oridationBiochemical and Biophysical Research Communications, 1992
- Marked elevation of urinary 3‐hydroxydecanedioic acid in a malnourished infant with glycogen storage disease, mimicking long‐chainl‐3‐hydroxyacyl‐CoA dehydrogenase deficiencyJournal of Inherited Metabolic Disease, 1992
- Combined enzyme defect of mitochondrial fatty acid oxidation.Journal of Clinical Investigation, 1992
- Fatty acid oxidation disorders: A new class of metabolic diseasesThe Journal of Pediatrics, 1992
- Hepatobiliary complications in patients with human immunodeficiency virus infectionThe American Journal of Medicine, 1992
- Long‐chain 3‐hydroxyacyl‐CoA dehydrogenase deficiency: Identification of a new inborn error of mitochondrial fatty acidβ‐oxidationJournal of Inherited Metabolic Disease, 1990
- Acquired immunodeficiency syndrome cholangiopathy: Spectrum of diseaseThe American Journal of Medicine, 1989
- HIV as a cause of giant cell hepatitisHuman Pathology, 1988