Nonimmune hydrops fetalis caused by G6PD deficiency hemolytic crisis and congenital dyserythropoietic anemia

被引:3
|
作者
Molad, M. [1 ,2 ]
Waisman, D. [1 ,2 ]
Rotschild, A. [1 ,2 ]
Auslander, R. [2 ,3 ]
Kessel, I. [1 ,2 ]
Soloviechick, M. [1 ,2 ]
Goldberg, Y. [2 ,3 ]
Shabad, E. [2 ,4 ]
机构
[1] Technion Israel Inst Technol, Carmel Med Ctr, Dept Neonatol, IL-34362 Haifa, Israel
[2] Technion Israel Inst Technol, Fac Med, IL-34362 Haifa, Israel
[3] Technion Israel Inst Technol, Carmel Med Ctr, Dept Obstet & Gynecol, IL-34362 Haifa, Israel
[4] Technion Israel Inst Technol, Carmel Med Ctr, Pediat Hematol Unit, IL-34362 Haifa, Israel
关键词
hemolysis; phototherapy; total blood exchange transfusion; congenital anemia; neonatal jaundice; ERYTHROCYTE G-6-PD DEFICIENCY; MATERNAL INGESTION; FAVA BEANS; NEWBORN;
D O I
10.1038/jp.2012.116
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
We present a case of a female neonate who had a nonimmune hydrops fetalis and severe hemolytic anemia due to a rare combination of glucose-6-phosphate dehydrogenase (G6PD) deficiency and congenital dyserythropoietic anemia. We conclude that in severe cases with persistent anemia one should search after delivery for a second reason other than G6PD deficiency alone.
引用
收藏
页码:490 / 491
页数:2
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