A case of atypical hemolytic uremic syndrome with a transient decrease in complement factor H

被引：3

作者：

Hahn, H ^{[1
]}

Um, EY

Park, YS

Cheong, HI

机构：

[1] Eulji Univ, Sch Med, Dept Pediat, Taejon, South Korea

[2] Seoul Natl Univ, Coll Med, Dept Pediat, Clin Res Inst, Seoul, South Korea

[3] Univ Ulsan, Coll Med, Dept Pediat, Ulsan 680749, South Korea

来源：

PEDIATRIC NEPHROLOGY | 2006年 / 21卷 / 02期

关键词：

complement; 3; complement factor H; hemolytic-uremic syndrome;

D O I：

10.1007/s00467-005-2108-1

中图分类号：

R72 [儿科学];

学科分类号：

100202 ;

摘要：

We report a case of sporadic atypical hemolytic uremic syndrome (HUS) with a transient decrease in complement factor H. Referred for hemolysis and azotemia without diarrhea prodrome, this 31-month-old boy showed a decreased complement 3 (C3) and complement factor H (FH) level. However, the factor H gene (HF1) mutation was missing. After the hemolysis was controlled with plasma infusion, the C3 and FH levels recovered. The patient's renal function fully recovered and remained normal, and there was no recurrence of the HUS.

引用

页码：295 / 298

页数：4

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