Fecteau G, Zinkl J G, Smith B P, O'Neil S, Smith S, Klopfer S
Département de sciences cliniques, Faculté de médecine véterinaire, Université de Montréal, Saint-Hyacinthe (Québec).
Can Vet J. 1997 Jul;38(7):443-4.
Hereditary fibrinogen deficiency is a rare condition in all species. Measurement of plasma fibrinogen should indicate low levels. Specific factor assays and pedigree analysis are essential in establishing a definitive diagnosis of the hereditary deficiency. Differentiation between afibrinogenemia, hypofibrinogenemia, and dysfibrinogenemia requires sophisticated techniques and assistance from a specialized laboratory.
遗传性纤维蛋白原缺乏症在所有物种中都是一种罕见的病症。血浆纤维蛋白原的检测结果应显示水平较低。特定因子检测和系谱分析对于明确遗传性缺乏症的诊断至关重要。无纤维蛋白原血症、低纤维蛋白原血症和异常纤维蛋白原血症之间的鉴别需要复杂的技术以及专业实验室的协助。
