1994 Feb;19(2):339-45. Links Acute gold n plump fatty acids
plump lips , laparoscopy, splenomegaly, plump teens , busty plump , nurses, fatty ratty , perinatalogy, queen fat bottomed girls , liverdisorders in pregnancy, plump woman , bay area, plump teen , cancer, edema, plump , plump thighs , fatty acids, We hypothesize that the interaction of an affected fetus with a female heterozygous for this defect in fatty acid oxidation in the late third trimester accounts for some cases of acute fatty liver of pregnancy.Publication Types: Case Reports PMID: 8294091 [PubMed - indexed for MEDLINE]  Display  Summary Brief Abstract Citation MEDLINE XML UI List LinkOut ASN.1 Related Articles Cited Articles Cited in Books CancerChrom Links Domain Links 3D Domain Links GEO DataSet Links Gene Links Gene (GeneRIF) Links Genome gold n plump Links Project Links GENSAT Links GEO Profile Links HomoloGene gold n plump Links gold n plump Nucleotide Links OMIA Links OMIM (calculated) Links OMIM (cited) Links BioAssay Links Compound Links Compound via MeSH Substance Links Substance via MeSH PMC Links Cited in PMC PopSet Links Probe Links Protein Links SNP Links Structure Links UniGene Links UniSTS Links  Show  5 10 20 50 100 200 500 Sort by Pub Date First Author Last Author Journal Send to Text File Printer Clipboard E-mail Order Write to the Help Desk NCBI | NLM | NIH Department of Health & Human Services Privacy
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1994 Feb;19(2):339-45. Links Acute fatty liver of pregnancy and fatty acids long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency.Treem WR, Rinaldo P, Hale DE, Stanley CA, Millington DS, Hyams JS, Jackson S, Turnbull DM.Division of Pediatric Gastroenterology, Hartford Hospital, Farmington, Connecticut 06115.The pathogenesis of acute fatty liver of pregnancy is unknown, but similarities in the clinical presentation fatty acids and the histological appearance of the liver with those found in children with metabolic defects in the intramitochondrial beta-oxidation pathway of the liver suggest that a disturbance fatty acids in hepatic fatty acid oxidation may play a role. We report a woman with acute fatty liver of pregnancy who gave birth to a seemingly normal full-term infant who was seen at 4 mo of age with hypoglycemia, coma and profound hepatic steatosis. The infant had a defect in fatty acid oxidation, long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency, and the mother proved to be heterozygous for this metabolic condition.
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