凝血因子能够从血浆中分离，用于治疗凝血因子缺乏的患者，如血友病。
Coagulation factors can be removed from plasma and may be used to treat people with coagulation factor deficiencies, such as hemophilia.
血友病患者的血液中缺乏凝血因子 VIII。
目的：探讨原发性系统性淀粉样变性并发凝血因子x缺乏的临床特征、发病机制及治疗方法。
Objective: to investigate the clinical feature, pathogenesis, and therapy of Primary systemic amyloidosis with acquired factor-X deficiency.
结论：凝血因子XII缺乏症是与习惯性流产有关联。其他因素数据，不能表明和习惯性流产的关系，或者这种关联是受限制的。
CONCLUSION: factor XII deficiency is associated with recurrent miscarriage. Data on the other factors either fail to show association or are quite limited.
新鲜冷冻血浆及冷沉淀物(常简称为冷沉淀)可输给凝血因子异常或缺乏的患者(比如，血友病患者)。
Fresh frozen plasma (FFP) and cryoprecipitate, often called "cryo" for short, are transfused to patients who have abnormal or low levels of blood clotting proteins, such as in hemophilia.
在典型的血友病中缺乏的是凝血因子VIII；其它的血友病是因缺乏凝血因子IX或XI。
Lack of factor VIII causes classic hemophilia; other types are caused by deficiency of factor IX or XI.
本课题在对具有先天性出血倾向的门诊患者进行筛查的过程中，发现了一例重型凝血因子V缺乏症患者。
The mutations in patients with factor V deficiency were identified including point mutation, frameshift mutation, deletion and insertion mutation.
凝血因子XIII缺乏症患者顾名思义，就是不能生成足够的凝血因子XIII，而凝血因子XIII在血液中循环，是参与正常的凝血的重要一个成分。
Patients with congenital Factor XIII deficiency don't make enough Factor XIII, a substance that circulates in the blood and is important for normal clotting.
血友病：一种遗传性出血性疾病，因先天性缺乏某种凝血因子而引起。
Hemophilia: Hereditary Bleeding disorder caused by deficiency of a coagulation factor.
血友病：一种遗传性出血性疾病，因先天性缺乏某种凝血因子而引起。
Hemophilia: Hereditary Bleeding disorder caused by deficiency of a coagulation factor.
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