儿童血友病的诊断与治疗

儿童血友病的诊断与治疗

血友病是一种遗传性出血性疾病,包括血友病A和血友病B,分别称为凝血因子Ⅷ（FⅧ）和凝血因子Ⅸ（FⅨ）缺乏,是由于FⅧ/FⅨ基因突变所引起的X-连锁隐性遗传性疾病。据世界血友病联盟（WFH）统计,全球重型及中型血友病患者共有35万人。近年随着生活水平的提高,诊治水平的发展,患者寿命的延长,血友病发病率有所上升。...

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Veröffentlicht in:Zhongguo xiang cun yi sheng 2011, Vol.13 (6), p.3-6
1. Verfasser: 吴润晖
Format: Artikel
Sprache:chi
Schlagworte:
X-连锁隐性遗传性疾病
世界血友病联盟
儿童
治疗
血友病B
血友病患者
诊断
遗传性出血性疾病
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creator 吴润晖
description 血友病是一种遗传性出血性疾病,包括血友病A和血友病B,分别称为凝血因子Ⅷ（FⅧ）和凝血因子Ⅸ（FⅨ）缺乏,是由于FⅧ/FⅨ基因突变所引起的X-连锁隐性遗传性疾病。据世界血友病联盟（WFH）统计,全球重型及中型血友病患者共有35万人。近年随着生活水平的提高,诊治水平的发展,患者寿命的延长,血友病发病率有所上升。
doi_str_mv 10.3969/j.issn.1007-614x.2011.06.001
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subjects X-连锁隐性遗传性疾病
世界血友病联盟
儿童
治疗
血友病B
血友病患者
诊断
遗传性出血性疾病
title 儿童血友病的诊断与治疗
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