目的对一个遗传性异常纤维蛋白原血症家系进行表型和基因型分析。
Objective To analyze the phenotype and genotype of a family with inherited dysfibrinogenemia.
最常见的凝血异常是纤维蛋白原转化为纤维蛋白障碍，TT（85%病例）和RT（90%）病例延长。
The most frequent clotting anomaly was defective fibrinogen conversion to fibrin, as demonstrated by prolongation of both TT (85% of cases) and RT (90% of cases).
表明纤维蛋白原结合唾液酸的水平可作为诊断肝硬化获得性异常纤维蛋白血症的理想指标。
Polymerization of fibrin monomer was inverse ratio with fibrinogen bound sialic acid. It suggests that fibrinogen boud sialic acid levels may be diagnostic index acquired dysfibrinogenaemia.
表明纤维蛋白原结合唾液酸的水平可作为诊断肝硬化获得性异常纤维蛋白血症的理想指标。
Polymerization of fibrin monomer was inverse ratio with fibrinogen bound sialic acid. It suggests that fibrinogen boud sialic acid levels may be diagnostic index acquired dysfibrinogenaemia.
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