n.异常纤维蛋白原血症

Dysfibrinogenemia is a rare bleeding disorder characterized by abnormal fibrinogen levels.
这是一种罕见的出血性疾病，其特征是纤维蛋白原水平异常。
The diagnosis of dysfibrinogenemia was confirmed through a blood test.
通过血液检查确认了血纤蛋白原不正常的情况。
Patients with dysfibrinogenemia often present with prolonged bleeding after injury or surgery.
患有血纤蛋白原异常的人在受伤或手术后常常出现长时间出血。
Treatment for dysfibrinogenemia involves replacing the deficient fibrinogen with fresh frozen plasma.
对于血纤蛋白原异常的治疗通常包括使用新鲜冷冻血浆补充缺乏的纤维蛋白原。
This genetic condition leads to dysfibrinogenemia, making it crucial for early intervention.
这种遗传状况导致血纤蛋白原异常，因此早期干预至关重要。
She experienced heavy menstrual bleeding due to a complication of dysfibrinogenemia.
她因为血纤蛋白原异常并发症而经历严重的月经出血。
Hemostasis studies showed abnormally low fibrinogen levels in the patient with dysfibrinogenemia.
出血止血研究显示患者血纤蛋白原水平异常偏低。
Dysfibrinogenemia can be inherited, but it can also result from certain medical conditions.
血纤蛋白原异常可能是遗传的，但也可能由某些疾病引起。
Management of dysfibrinogenemia requires close collaboration between hematologists and primary care physicians.
对血纤蛋白原异常的管理需要血液科医生和全科医生的紧密合作。
A family history of dysfibrinogenemia prompted doctors to screen her children at an early age.
家族中有血纤蛋白原异常的历史促使医生建议她在孩子很小的时候进行筛查。