Massive acute haemolysis in neonates with glucose-6-phosphate dehydrogenase deficiency

Archives of Disease in Childhood: Fetal and Neonatal Edition

Volumn 88, Issue 6, 2003, Pages

  Dhillon, A S ^a   Darbyshire, P J ^b   Williams, M D ^b   Bissenden, J G ^c  

^a BIRMINGHAM WOMEN S HOSPITAL   (United Kingdom)

^b BIRMINGHAM CHILDREN S HOSPITAL   (United Kingdom)

^c CITY HOSPITAL   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

AMINOPHYLLINE; CAFFEINE CITRATE; CEFOTAXIME; GENTAMICIN; PENICILLIN G; PHYTOMENADIONE; VANCOMYCIN;

ARTICLE; CASE REPORT; CLINICAL FEATURE; DISEASE COURSE; EXCHANGE BLOOD TRANSFUSION; FEMALE; GLUCOSE 6 PHOSPHATE DEHYDROGENASE DEFICIENCY; HEMOLYSIS; HUMAN; LABORATORY TEST; MALE; NEWBORN; PRIORITY JOURNAL;

EID: 0344515323     PISSN: 13592998     EISSN: 14682052     Source Type: Journal    
DOI: 10.1136/fn.88.6.f534     Document Type: Article

References (24)

1. Beutler E. G6PD deficiency. Blood 1994;84:3613-36.
2. Kaplan M, Hammerman C. Severe neonatal hyperbilirubinemia. A potential complication of glucose-6-phosphate dehydrogenase deficiency. Clin Perinatol 1998;25:575-90.
3. Valaes T. Severe neonatal jaundice associated with glucose-6-phosphate dehydrogenase deficiency: Pathogenesis and global epidemiology. Acta Paediatr 1994;394(suppl):58-76.
4. Kaplan M, Beutler E, Vreman HJ, et al. Neonatal hyperbilirubinemia in glucose-6-phosphate dehydrogenase-deficient heterozygotes. Pediatrics 1999;104:68-74.
5. Iolascon A, Faienza MF, Perrotta S, et al. Gilbert's syndrome and jaundice in glucose-6-phosphate dehydrogenase deficient neonates. Haematologica 1999;84:99-102.
6. Eshaghpour E, Oski FA, Williams M. The relationship of erythrocyte glucose-6-phosphate dehydrogenase deficiency to hyperbilirubinaemia in Negro premature infants. J Pediatr 1967;70:595-601.
7. Valaes T, Karaklis A, Stravrakakis D, et al. Incidence and mechanism of neonatal jaundice related to glucose-6-phosphate deficiency. Pediatr Res 1969;3:448-58.
8. Kaplan M, Vreman HJ, Hammerman C, et al. Contribution of haemolysis to jaundice in Sephardic Jewish glucose-6-phosphate dehydrogenase deficient neonates. Br J Haematol 1996;93:822-7.
9. Necheles TF, Rai US, Valaes T. The role of hemolysis in neonatal hyperbilirubinaemia as reflected in carboxyhaemoglobin levels. Acta Paediatr Scand 1976;65:361-7.
10. Taj-Eldin S. Favism in breast-fed infants. Arch Dis Child 1971;46:121-3.
11. Zinkham WH. Peripheral blood and bilirubin values in normal full-term primaquine-sensitive negro infants: Effect of vitamin K. Pediatrics 1963;31:983-95.
12. Meloni T, Costa S, Cutillo S. Haptoglobin, hemopexin, hemoglobin and hematocrit in newborns with erythrocyte of glucose-6-phosphate dehydrogenase deficiency. Acta Haematol 1975;54:284-8.
13. Vulliamy TJ, Kaeda JS, Ait-Chafa D, et al. Clinical and haematological consequences of recurrent G6PD mutations and a single new mutation causing chronic nonspherocytic haemolytic anaemia. Br J Haematol 1998;101:670-5.
14. Vlachos A, Westwood B, Lipton JM, et al. G6PD Mount Sinai: a new severe hemolytic variant characterized by dual mutations at nucleotides 376G and 1159T (N126D). Hum Mutat 1998;(suppl 1):S154-5.
15. Ainoon O, Joyce J, Boo NY, et al. Glucose-6-phosphate dehydrogenase (G6PD) variants in Malaysian Chinese. Hum Mut 1999;14:352.
16. 51-labeled erythrocytes. Pediatrics 1961;27:354-61.
17. Mentzer WC Jr, Collier E. Hydrops fetalis associated with erythrocyte G-6-PD deficiency and maternal ingestion of fava beans and ascorbic acid. J Pediatr 1975;86:565-7.
18. Valaes T, Doxiadis SA, Fessas P. Acute hemolysis due to naphthalene inhalation. J Pediatr 1963;63:904-15.
19. Lucey JF, Dolan RG. Hyperbilirubinaemia of newborn infants associated with parenteral administration of a vitamin K analogue to the mothers. Pediatrics 1959;23:553-60.
20. Kaplan M, Waisman D, Mazor D, et al. Effect of vitamin K1 on glucose-6-phosphate dehydrogenase deficient neonatal erythrocytes in vitro. Arch Dis Child Fetal Neonatal Ed 1998;79:F218-20.
21. Ballin A, Brown EJ, Koren G, et al. Vitamin C-induced erythrocyte damage in premature infants. J Pediatr 1988;113:114-20.
22. Squire R, Kiely E, Drake D, et al. Intravascular haemolysis in association with necrotising enterocolitis. J Pediatr Surg 1992;27:808-10.
23. Osborn DA, Lui K, Pussell P, et al. T and Tk antigen activation in necrotising enterocolitis: manifestations, severity of illness, and effectiveness of testing. Arch Dis Child Fetal Neonatal Ed 1999;80:F192-7.
24. Sethi S, Dhingra N, Madan N, et al. Erythrocyte T-activation: clinical importance and recognition by a simple routine technique. Ind J Path Microbiol 1994;37:109-11.