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对三名因异常类型的凝血因子IX导致患克里斯马斯病的患者进行的调查。

An investigation of three patients with Christmas disease due to an abnormal type of factor IX.

作者信息

Denson K W, Biggs R, Mannucci P M

出版信息

J Clin Pathol. 1968 Mar;21(2):160-5. doi: 10.1136/jcp.21.2.160.

Abstract

Three patients with Christmas disease whose plasma was shown to have a prolonged one-stage prothrombin time with ox brain thromboplastin have been investigated. These patients have an inhibitor for the reaction between factor X, factor VII, and ox brain extract. The abnormal constituent responsible for this inhibitor appears to be factor IX whuch is functionally inactive but antigenically indistinguishable from normal factor IX. It is proposed that patients might be classified into haemophilia B(+) for patients with this defect (Christmas disease(+)) and haemophilia B(-) (Christmas disease(-)) for patients who have classical Christmas disease.

摘要

对三名患有克里斯马斯病的患者进行了研究,他们的血浆在用牛脑凝血活酶时显示一期凝血酶原时间延长。这些患者体内存在一种抑制因子X、因子VII与牛脑提取物之间反应的物质。导致这种抑制作用的异常成分似乎是因子IX,其功能失活,但在抗原性上与正常因子IX无法区分。建议将患有这种缺陷的患者(克里斯马斯病阳性)归类为血友病B(+),而将患有典型克里斯马斯病的患者归类为血友病B(-)(克里斯马斯病阴性)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c2b5/473716/68db2537287c/jclinpath00373-0046-a.jpg

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