Acute hemolysis and severe neonatal hyperbilirubinemia in glucose-6-phosphate dehydrogenase-deficient heterozygotes

被引：39
|
作者：
Kaplan, M [1 ]
Hammerman, C
Vreman, HJ
Stevenson, DK
Beutler, E
机构：
[1] Shaare Zedek Med Ctr, Dept Neonatol, IL-91031 Jerusalem, Israel
[2] Hebrew Univ Jerusalem, Fac Med, Jerusalem, Israel
[3] Stanford Univ, Med Ctr, Div Pediat, Neonatal & Dev Metab Lab, Stanford, CA 94305 USA
[4] Scripps Res Inst, Dept Mol & Expt Med, La Jolla, CA USA
来源：
JOURNAL OF PEDIATRICS | 2001年 / 139卷 / 01期
关键词：
D O I：
10.1067/mpd.2001.115312
中图分类号：
R72 [儿科学];
学科分类号：
100202 ;
摘要：
Two premature female infants had severe hyperbilirubinemia caused by hemolysis. Both neonates were heterozygotes for the glucose-g-phosphate dehydrogenase Mediterranean mutation as determined by DNA analysis. Glucose-6-phosphate dehydrogenase-deficient heterozygotes may be susceptible to the complications of this enzyme deficiency.
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页码：137 / 140
页数：4
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