[因子VII缺乏性低转化性贫血]。

Bilten za hematologiju i transfuziju Pub Date : 1979-01-01
P Martinić, B Brusić
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引用次数: 0

摘要

先天性第七因子缺陷是一种罕见的缺陷,认为在妇女和男子。临床表现为轻度出血症状和实验室检查:凝血酶原时间延长,凝血因子7活性降低,APTT正常。在本文中,我们描述了我们发现的两例先天性七因子缺陷的家庭,生化特征,鉴别实验室诊断和出血情况下缺陷的纠正。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Factor VII deficit-hypoconvertinemia].

Congenital deficit of Factor VII is a rare deficit perceived within women and men. Clinicaly it is manifested with mild hemoragical diatesa and of laboratory tests: prolonged on stage prothrombin time, reduced activity of Factor VII and normal APTT. In this article we describe the family in which we have found two cases of congenital deficit of Factor VII, biochemical characteristics, differential laboratory diagnosis and correction of deficit in the case of bleeding.

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