Nonimmune hydrops fetalis due to congenital xerocytosis

被引：4

作者：

Vicente-Guitiérrez M.P. ^{[1
]}

Castelló-Almazán I. ^{[1
]}

Salvía-Roiges M.D. ^{[2
]}

Rodríguez-Miguélez J.M. ^{[2
]}

Vives-Corrons J.-L. ^{[3
]}

Figueras-Aloy J. ^{[2
]}

Carbonell-Estrany X. ^{[2
]}

机构：

[1] Unitat Integrada de Pediatria, Clinic-Hospital Sant Joan de Deu, Esplugues de Llobregat, Barcelona

[2] Servei de Neonatologia, Institut Clinic de Ginecologia, Hospital Clínic, Barcelona

[3] Unitat de Patologia Eritrocitaria, Hospital Clínic, Barcelona

来源：

Journal of Perinatology | 2005年 / 25卷 / 1期

关键词：

D O I：

10.1038/sj.jp.7211200

中图分类号：

学科分类号：

摘要：

Hereditary xerocytosis is a rare hemolytic anemia in which erythrocytes are dehydrated due to a loss of potassium and water through their cell wall membrane. In adults, this condition leads, to a mild-to-moderate hemolysis. We report a case of hydrops fetatis secondary to hereditary xerocytosis. Management with intrauterine erthrocyte and albumin transfusions resulted in a favorable postnatal course. © 2005 Nature Publishing Group All rights reserved.

引用

页码：63 / 65

页数：2

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