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Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency—diagnosis, plasma carnitine fractions and management in a further patient

✍ Scribed by R. Moore; J. F. T. Glasgow; M. A. Bingham; J. A. Dodge; R. J. Pollitt; S. E. Olpin; B. Middleton; K. Carpenter


Book ID
105413214
Publisher
Springer
Year
1993
Tongue
English
Weight
454 KB
Volume
152
Category
Article
ISSN
0340-6997

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The pathogenesis of acute fatty liver of pregnancy is unknown, but similarities in the clinical presentation and the histological appearance of the liver with those found in children with metabolic defects in the intramitochondrial fboxidation pathway of the liver suggest that a disturbance in hepat