Familial recurrent hemolytic uremic syndrome

被引：0

作者：

Ben Becher, S ^{[1
]}

Cheour, M ^{[1
]}

Joulak, M ^{[1
]}

Kammoun, A ^{[1
]}

Ben Moussa, F ^{[1
]}

Lakhoua, R ^{[1
]}

Boudhina, T ^{[1
]}

机构：

[1] Hop Enfants, Serv Pediat Urgences & Consultat Externes, Tunis, Tunisia

来源：

ANNALES DE PEDIATRIE | 1997年 / 44卷 / 09期

关键词：

hemolytic uremic syndrome; inherited diseases; recurrences; clinical features; outcome; histology; child;

D O I：

暂无

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

Four siblings had one or more episodes of hemolytic uremic syndrome. One was a boy who had two episodes, at 3 1/2 and 8 years of age, respectively. One of his sisters had five episodes, at three years of age, then every year from 6 to 9 years of age. The remaining sister and brother each had one episode, at 3 years 8 months and 4 years 8 months of age, respectively. The outcome was favorable in all four cases. Histologic features varied from one sibling to the next.

引用

页码：601 / 605

页数：5

共 23 条

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