Glucose-6-phosphate dehydrogenase deficiency in triplets of African-American descent

被引:0
作者
H K Turbendian
J M Perlman
机构
[1] Weill Cornell University,Division of Newborn Medicine
来源
Journal of Perinatology | 2006年 / 26卷
关键词
glucose 6 phosphate dehydrogenase deficiency; jaundice; triplets; premature;
D O I
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学科分类号
摘要
Despite the prevalence of glucose-6-phosphate dehydrogenase (G6PD) deficiency in African Americans, the disorder maybe often overlooked as a diagnosis in the absence of overt signs of hemolysis in neonates with hyperbilirubinemia. We present a case report of anemia and prolonged hyperbilirubinemia due to G6PD deficiency in the absence of hemolysis in dichorionic, triamniotic, preterm triplets of African-American descent.
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页码:201 / 203
页数:2
相关论文
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[1]  
MacDonald MG(1995)Hidden risks: early discharge and bilirubin toxicity due to glucose-6-phosphate dehydrogenase deficiency Pediatrics 96 734-738
[2]  
Washington EC(1995)Hemolytic jaundice due to G6PD deficiency causing kernicterus in a female newborn South Med J 88 776-779
[3]  
Ector W(2004)Hyperbilirubinemia among African American, glucose-6-phosphate dehydrogenase-deficient neonates Pediatrics 114 E213-E219
[4]  
Abboud M(1960)Methaemoglobin Reduction Test Bull WHO 22 633-640
[5]  
Ohning B(2003)Bilirubin toxicity in the developing nervous system Pediatr Neurol 29 410-421
[6]  
Holden K(2003)Massive acute haemolysis in neonates with glucose-6-phosphate dehydrogenase deficiency Arch Dis Child Fetal Neonatal Ed 88 534-536
[7]  
Kaplan M(2005)Poor correlation between hemolysis and jaundice in glucose 6-phosphate dehydrogenase-deficient babies Pediatr Int 47 258-261
[8]  
Herschel M(1996)Contribution of haemolysis to jaundice in Sephardic Jewish glucose-6-phosphate dehydrogenase deficient neonates Br J Haematol 93 822-827
[9]  
Hammerman C(1995)Role of hemolysis in neonatal jaundice associated with glucose-6 phosphate dehydrogenase deficiency J Pediatr 127 804-806
[10]  
Hoyer J(2001)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 Mol Dis 27 918-923