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

来源：

JOURNAL OF PERINATOLOGY | 2013年 / 33卷 / 06期

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

页码：490 / 491

页数：2

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