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- W2062290772 endingPage "824" @default.
- W2062290772 startingPage "815" @default.
- W2062290772 abstract "Since the first report of long-chain L-3-hydroxyacyl-coenzyme A dehydrogenase deficiency a little more than a decade ago, its phenotypic and genotypic heterogeneity in individuals homozygous for the enzyme defect has become more and more evident. Even more interesting is its association with pregnancy-specific disorders, including preeclampsia, HELLP syndrome (hemolysis, elevated liver enzymes, low platelets), hyperemesis gravidarum, acute fatty liver of pregnancy, and maternal floor infarct of the placenta. In this review we discuss the biochemical and molecular basis, clinical features, diagnosis, and management of long-chain L-3-hydroxyacyl-coenzyme A dehydrogenase deficiency." @default.
- W2062290772 created "2016-06-24" @default.
- W2062290772 creator A5031711759 @default.
- W2062290772 creator A5032313369 @default.
- W2062290772 creator A5087592000 @default.
- W2062290772 date "2002-07-01" @default.
- W2062290772 modified "2023-10-18" @default.
- W2062290772 title "Long-Chain L-3-Hydroxyacyl-Coenzyme A Dehydrogenase Deficiency: A Molecular and Biochemical Review" @default.
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