hyperfibrinogenemia testing
纤维原血症检测
diagnosing hyperfibrinogenemia
诊断纤维原血症
hyperfibrinogenemia levels
纤维原血症水平
with hyperfibrinogenemia
伴有纤维原血症
hyperfibrinogenemia risk
纤维原血症风险
hyperfibrinogenemia study
纤维原血症研究
hyperfibrinogenemia cases
纤维原血症病例
hyperfibrinogenemia syndrome
纤维原血症综合征
hyperfibrinogenemia found
发现纤维原血症
severe hyperfibrinogenemia
重度纤维原血症
doctors are investigating the patient's hyperfibrinogenemia to rule out potential clotting risks.
医生正在调查患者的超高纤维蛋白原血症，以排除潜在的凝血风险。
genetic testing revealed a predisposition to hyperfibrinogenemia in the family.
基因检测显示该家族有患超高纤维蛋白原血症的易感性。
the diagnostic workup included assessing for hyperfibrinogenemia and other coagulation disorders.
诊断工作包括评估超高纤维蛋白原血症和其他凝血功能障碍。
patients with hyperfibrinogenemia may experience an increased risk of deep vein thrombosis.
患有超高纤维蛋白原血症的患者可能面临更高的深静脉血栓风险。
further research is needed to understand the long-term implications of hyperfibrinogenemia.
需要进一步研究以了解超高纤维蛋白原血症的长期影响。
the lab results confirmed the presence of hyperfibrinogenemia, warranting further investigation.
实验室结果证实了超高纤维蛋白原血症的存在，需要进一步调查。
anticoagulant medications may be prescribed to manage hyperfibrinogenemia and prevent complications.
可能开具抗凝药物来控制超高纤维蛋白原血症并预防并发症。
monitoring fibrinogen levels is crucial in patients suspected of having hyperfibrinogenemia.
在怀疑患有超高纤维蛋白原血症的患者中，监测纤维蛋白原水平至关重要。
the severity of hyperfibrinogenemia can vary significantly among individuals.
超高纤维蛋白原血症的严重程度因人而异。
a detailed medical history is essential when evaluating patients with suspected hyperfibrinogenemia.
在评估疑似患有超高纤维蛋白原血症的患者时，详细的病史至关重要。
the patient's hyperfibrinogenemia was discovered during a routine blood test.
患者的超高纤维蛋白原血症是在常规血液检查中发现的。
hyperfibrinogenemia testing
纤维原血症检测
diagnosing hyperfibrinogenemia
诊断纤维原血症
hyperfibrinogenemia levels
纤维原血症水平
with hyperfibrinogenemia
伴有纤维原血症
hyperfibrinogenemia risk
纤维原血症风险
hyperfibrinogenemia study
纤维原血症研究
hyperfibrinogenemia cases
纤维原血症病例
hyperfibrinogenemia syndrome
纤维原血症综合征
hyperfibrinogenemia found
发现纤维原血症
severe hyperfibrinogenemia
重度纤维原血症
doctors are investigating the patient's hyperfibrinogenemia to rule out potential clotting risks.
医生正在调查患者的超高纤维蛋白原血症，以排除潜在的凝血风险。
genetic testing revealed a predisposition to hyperfibrinogenemia in the family.
基因检测显示该家族有患超高纤维蛋白原血症的易感性。
the diagnostic workup included assessing for hyperfibrinogenemia and other coagulation disorders.
诊断工作包括评估超高纤维蛋白原血症和其他凝血功能障碍。
patients with hyperfibrinogenemia may experience an increased risk of deep vein thrombosis.
患有超高纤维蛋白原血症的患者可能面临更高的深静脉血栓风险。
further research is needed to understand the long-term implications of hyperfibrinogenemia.
需要进一步研究以了解超高纤维蛋白原血症的长期影响。
the lab results confirmed the presence of hyperfibrinogenemia, warranting further investigation.
实验室结果证实了超高纤维蛋白原血症的存在，需要进一步调查。
anticoagulant medications may be prescribed to manage hyperfibrinogenemia and prevent complications.
可能开具抗凝药物来控制超高纤维蛋白原血症并预防并发症。
monitoring fibrinogen levels is crucial in patients suspected of having hyperfibrinogenemia.
在怀疑患有超高纤维蛋白原血症的患者中，监测纤维蛋白原水平至关重要。
the severity of hyperfibrinogenemia can vary significantly among individuals.
超高纤维蛋白原血症的严重程度因人而异。
a detailed medical history is essential when evaluating patients with suspected hyperfibrinogenemia.
在评估疑似患有超高纤维蛋白原血症的患者时，详细的病史至关重要。
the patient's hyperfibrinogenemia was discovered during a routine blood test.
患者的超高纤维蛋白原血症是在常规血液检查中发现的。
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