Low glucose-6-phosphate dehydrogenase enzyme activity level at the time of hemolysis in a male neonate with the African type of deficiency

Blood Cells, Molecules, and Diseases

Volumn 27, Issue 5, 2001, Pages 918-923

  Herschel, Marguerite ^a   Beutler, Ernest ^b  

^a UNIVERSITY OF CHICAGO   (United States)

^b SCRIPPS RESEARCH INSTITUTE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

GENE PRODUCT; GLUCOSE 6 PHOSPHATE DEHYDROGENASE; GLUCURONOSYLTRANSFERASE; GLUCURONOSYLTRANSFERASE 1A1; UNCLASSIFIED DRUG; BILIRUBIN URIDINE DIPHOSPHOGLUCURONOSYL TRANSFERASE 1A1; BILIRUBIN URIDINE-DIPHOSPHOGLUCURONOSYL TRANSFERASE 1A1;

ARTICLE; BILE ACID SYNTHESIS; CASE REPORT; DISEASE ASSOCIATION; DNA DETERMINATION; ENZYME ACTIVITY; GENETIC POLYMORPHISM; GILBERT DISEASE; GLYCOGEN STORAGE DISEASE TYPE 1; HEMOLYSIS; HUMAN; HYPERBILIRUBINEMIA; MALE; NEGRO; NEWBORN; NEWBORN DISEASE; NEWBORN JAUNDICE; PRIORITY JOURNAL; PROMOTER REGION; BLOOD; ENZYMOLOGY; GENETIC VARIABILITY; GENETICS; GLUCOSE 6 PHOSPHATE DEHYDROGENASE DEFICIENCY;

BLACKS; CASE REPORT; GILBERT DISEASE; GLUCOSEPHOSPHATE DEHYDROGENASE; GLUCOSEPHOSPHATE DEHYDROGENASE DEFICIENCY; GLUCURONOSYLTRANSFERASE; HEMOLYSIS; HUMAN; INFANT, NEWBORN; JAUNDICE, NEONATAL; MALE; PROMOTER REGIONS (GENETICS); SUPPORT, NON-U.S. GOV'T; SUPPORT, U.S. GOV'T, P.H.S.; VARIATION (GENETICS);

EID: 0035210914     PISSN: 10799796     EISSN: None     Source Type: Journal    
DOI: 10.1006/bcmd.2001.0467     Document Type: Article

References (35)

1. Hidden risks: Early discharge and bilirubin toxicity due to glucose-6-phosphate dehydrogenase deficiency
2. Hemolytic jaundice due to G6PD deficiency causing kernicterus in a female newborn
3. Commentary. Glucose-6-phosphate dehydrogenase-deficient neonates: A potential cause for concern in North America
4. The blood and hematopoietic system
5. Gilbert's syndrome and glucose-6-phosphate dehydrogenase deficiency: A dose-dependent genetic interaction crucial to neonatal hyperbilirubinemia
6. Neonatal hyperbilirubinemia in glucose-6-phosphate dehydrogenase-deficient heterozygotes
7. Carbon monoxide and carboxyhemoglobin
8. Yield of reticulocyte counts and blood smears in term infants
9. Glucose-6-phosphate dehydrogenase deficiency
10. Comparison of the direct Coombs' antiglobulin test (DAT) for identification of newborns at-risk or not-at-risk for hemolysis with a known indicator of the rate of hemolysis, the end-tidal carbon monoxide (CO) concentration in parts per million (ppm) corrected for inhaled CO (ETCOc)
11. End-tidal carbon monoxide (ETCOc) hour-specific nomogram for early and pre-discharge identification of babies with increased bilirubin production
12. DNA sequence abnormalities of human glucose-6-phosphate dehydrogenase variants
13. Racial variability in the UDP-glucuronosyltransferase 1 (UGT1A1) promoter: A balanced polymorphism for regulation of bilirubin metabolism?
14. Bilirubin conjugation, reflected by conjugated bilirubin fractions, in glucose-6-phosphate dehydrogenase-deficient neonates: A determining factor in the pathogenesis of hyperbilirubinemia
15. The hemolytic effect of primaquine. IV. The relationship of cell age to hemolysis
16. Enzymatic deficiency in primaquine-sensitive erythrocytes
17. Glucose-6-phosphate dehydrogenase deficiency
18. In vivo lability of glucose-6-phosphate dehydrogenase in GdA- and Gd Mediterranean deficiency
19. How do red cell enzymes age? Hypothesis and facts
20. The hemolytic effect of primaquine. VIII. The effect of drug administration on parameters of primaquine sensitivity
21. Acute hemolytic anemia in the newborn infant due to naphthalene poisoning: Report of two cases, with investigations into the mechanism of the disease
22. A simple visual screening test for glucose-6-phosphate dehydrogenase deficiency employing ascorbate and cyanide
23. Primaquine sensitivity in Caucasians: Hemolytic reactions induced by primaquine in G-6-PD deficient subjects
24. Glucose-6 phosphate dehydrogenase deficiency, infectious hepatitis, acute hemolysis, and renal failure
25. Clinical and biochemical interactions of glucose-6-phosphate dehydrogenase deficiency and sickle-cell anemia
26. Prevalence of glucose-6-phosphate dehydrogenase deficiency in sickle-cell disease
27. Population genetics of glucose-6-phosphate dehydrogenase deficiency of the red cell
28. Acute hemolytic anemia complicating viral hepatitis in patients with glucose-6-phosphate dehydrogenase deficiency
29. Studies of glucose 6-phosphate dehydrogenase activity of individual erythrocytes: The methaemoglobin elution test for identification of females heterozygous for G6PD deficiency
30. A tetrazolium-linked cytochemical method for estimation of glucose-6-phosphate dehydrogenase activity in individual erythrocytes: Applications in the study of heterozygotes for glucose-6-phosphate dehydrogenase deficiency
31. Diagnosis of erythrocyte glucose-6-phosphate dehydrogenase deficiency in the Negro male despite hemolytic crisis
32. A simple laboratory procedure for the recognition of A- (African type) G-6-PD deficiency in acute haemolytic crisis
33. A sensitive cytochemical staining method for glucose-6-phosphate dehydrogenase activity in individual erythrocytes
34. Molecular heterogeneity of G6PD A-