
pmid: 17126586
Primary carnitine deficiency impairs fatty acid oxidation and can result in hypoglycemia, hepatic encephalopathy, cardiomyopathy and sudden death. We diagnosed primary carnitine deficiency in six unrelated women whose unaffected infants were identified with low free carnitine levels (C0) by newborn screening using tandem mass spectrometry. Given the lifetime risk of morbidity or sudden death, identification of adult patients with primary carnitine deficiency is an added benefit of expanded newborn screening programs.
Adult, Fatty Acids, Infant, Newborn, Lipid Metabolism Disorders, Infant, Neonatal Screening, Tandem Mass Spectrometry, Carnitine, Humans, Female, Genetic Testing, Oxidation-Reduction
Adult, Fatty Acids, Infant, Newborn, Lipid Metabolism Disorders, Infant, Neonatal Screening, Tandem Mass Spectrometry, Carnitine, Humans, Female, Genetic Testing, Oxidation-Reduction
| selected citations These citations are derived from selected sources. This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | 83 | |
| popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network. | Top 10% | |
| influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically). | Top 10% | |
| impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network. | Top 10% |
