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首页> 外文期刊>Open Journal of Blood Diseases >Factor XII (Hageman Factor) Deficiency: A Very Rare Coagulation Disorder
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Factor XII (Hageman Factor) Deficiency: A Very Rare Coagulation Disorder

机译:XII因子(Hageman因子)缺乏症:一种非常罕见的凝血障碍

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Background: Factor XII (Hageman Factor) is the initiating factor for the Intrinsic Pathway of Coagulation. Very low levels of Factor XII have been associated with increased levels of activated Partial Thromboplastin Time (aPTT). Association of Factor XII deficiency is more with thromboembolic disorders rather than bleeding tendencies. Aim: To learn more about the relationship of factor XII (Hageman Factor) deficiency and high levels of activated Partial Thromboplastin Time. Case Presentation: The Patient was admitted with complains of recurrent headaches and loin pain. Patient was incidentally found to have prolonged activated Partial Thromboplastin Time. This led to investigations which ultimately provided the evidence of severely low levels of Hageman Factor. Conclusion: Hageman Factor deficiency causes prolonged activated Partial Thromboplastin Time. However, most of the patients are asymptomatic for many years despite Hageman Factor deficiency.
机译:背景:XII因子(Hageman因子)是凝血固有途径的引发因子。极低水平的因子XII与活化的部分凝血活酶时间(aPTT)升高有关。凝血因子XII缺乏与血栓栓塞性疾病的关联更多,而不是出血倾向。目的:了解更多有关XII因子(Hageman因子)缺乏与高水平的活化部分凝血活酶时间的关系。病例介绍:患者因反复头痛和腰痛而入院。偶然发现患者激活了部分凝血活酶时间延长。这导致了调查,最终提供了哈格曼因子水平极低的证据。结论:Hageman因子缺乏会导致部分凝血活酶激活时间延长。但是,尽管缺乏哈格曼因子缺乏症,但大多数患者多年没有症状。

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