Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

A case of severe preeclampsia leading to the diagnosis of de novo abnormal fatty acid metabolism and ACE gene deletion.

Journal of obstetrics and gynaecology Canada : JOGC = Journal d'obstetrique et gynecologie du Canada : JOGC - 1 Jul 2010

Iruretagoyena Jesus I, Shah Dinesh

Abstract excerpt

BACKGROUND: Enzymes involved in the metabolism of free fatty acids are essential for the proper use of caloric intake. Abnormal enzymes unable to degrade fatty acids will result in an accumulation of fatty acids in organs like the liver, impairing its function. CASE: A 28-year-old primigravid woman underwent induction of labour because of severe preeclampsia. She was subsequently found to be a carrier for...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Fatty Acids
Share to Gene Deletion

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Homozygote

Share to Metabolism, Inborn Errors

Share to Peptidyl-Dipeptidase A

Share to Pre-Eclampsia

Share to Pregnancy

Share to Severity of Illness Index

Source

Identifiers

PMID: 20707960
DOI: 10.1016/s1701-2163(16)34575-3

Genes

ACE

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A case of severe preeclampsia leading to the diagnosis of de novo abnormal fatty acid metabolism and ACE gene deletion.PMID 20707960Read ↗

Acute Fatty Liver Disease of Pregnancy: Updates in Pathogenesis, Diagnosis, and ManagementSemantic proximity Read ↗

Recurrent acute fatty liver of pregnancy associated with a fatty-acid oxidation defect in the offspringSemantic proximity Read ↗

Acute fatty liver of pregnancy and neonatal long-chain 3-hydroxyacyl-coenzyme A dehydrogenase (LCHAD) deficiency.Semantic proximity Read ↗

Acute fatty liver disease of pregnancySemantic proximity Read ↗

Mitochondrial Dysfunction and Acute Fatty Liver of PregnancySemantic proximity Read ↗

Acute fatty liver of pregnancy (AFLP) – an overviewSemantic proximity Read ↗

Preeclampsia‐induced Liver Dysfunction, HELLP syndrome, and acute fatty liver of pregnancySemantic proximity Read ↗

Role of 3-Hydroxy Fatty Acid-Induced Hepatic Lipotoxicity in Acute Fatty Liver of Pregnancy.Semantic proximity Read ↗

Role of genetic screening in identifying susceptibility to acute fatty liver of pregnancy.Semantic proximity Read ↗

Assessment of the prevalence of genetic metabolic defects in acute fatty liver of pregnancySemantic proximity Read ↗

Differentiation of acute fatty liver of pregnancy from syndrome of hemolysis, elevated liver enzymes and low platelet countsSemantic proximity Read ↗

Acute fatty liver of pregnancy and long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency†Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.