Optimizing the treatment of haemophilia B: laboratory and clinical perspectives

被引：3
|
作者：
Aledort, L. M. [1 ]
机构：
[1] Mt Sinai Sch Med, New York, NY 10029 USA
来源：
HAEMOPHILIA | 2010年 / 16卷
关键词：
chromogenic assays; clotting assays; factor IX; haemophilia B; pharmacokinetics; prophylaxis; FACTOR-IX; FACTOR-VIII; SEVERITY;
D O I：
10.1111/j.1365-2516.2010.02298.x
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
Hemophilia A and B are traditionally thought of as a single bleeding disorder, viewed as opposite sides of the same coin. Yet the differences between the 2 forms of congenital hemophilia extend far beyond the type of deficient clotting factor-factor VIII for hemophilia A and factor IX (FIX) for hemophilia B. This supplement focuses on the unique laboratory and clinical issues associated with FIX replacement therapy for children and adults with hemophilia B.
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页码：1 / 2
页数：2
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