如何知道我有没有纤溶酶原缺乏症

什么症状应该引起您可能身患纤溶酶原缺乏症的疑虑?其他纤溶酶原缺乏症患者针对此事所给予的建议以及应该寻求什么专科医疗。

原本


Both clinical and blood laboratory findings are used to help identify if you or a loved one has congenital PLGD. To confirm or rule out the doctor’s suspicion, a variety of tests are available that can also help determine the extent and severity of the condition

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