The HELLP syndrome associated with fetal medium-chain acyl-CoA dehydrogenase deficiency

Journal of Inherited Metabolic Disease

Volumn 23, Issue 5, 2000, Pages 518-519

  Nelson, J ^a   Lewis, B ^a   Walters, B ^a  

^a KING EDWARD MEMORIAL HOSPITAL   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

3 HYDROXYACYL COENZYME A DEHYDROGENASE; ALANINE AMINOTRANSFERASE; FATTY ACID; HEMOGLOBIN; LIPOPROTEIN; URATE;

ADULT; ARTICLE; AUTOPSY; BLOOD ANALYSIS; CASE REPORT; CLINICAL FEATURE; DELIVERY; DISEASE ASSOCIATION; DISORDERS OF MITOCHONDRIAL FUNCTIONS; ENZYME DEFICIENCY; FATTY ACID METABOLISM; FEMALE; FETUS DISEASE; HELLP SYNDROME; HUMAN; NEWBORN; NEWBORN MORTALITY; PREECLAMPSIA; PREGNANCY TOXEMIA;

ACYL-COA DEHYDROGENASE; ACYL-COA DEHYDROGENASES; ADULT; FEMALE; FETAL DISEASES; HELLP SYNDROME; HUMANS; INFANT; INFANT, NEWBORN; LIPID METABOLISM, INBORN ERRORS; PRE-ECLAMPSIA; PREGNANCY;

EID: 0033941464     PISSN: 01418955     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1005676600975     Document Type: Article

References (3)

1. Postpartum plasma exchange for atypical pre-eclampsia-eclampsia as HELLP (hemolysis, elevated liver enzymes, and low platelets) syndrome
2. Potential pathogenic roles of aberrant lipo-protein and fatty acid metabolism in pre-eclampsia
3. Pregnancy complications are frequent in long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency