Thrombophilic Disorders
نویسندگان
چکیده
منابع مشابه
Inherited thrombophilic disorders
Inherited thrombophilia is thought to increase the risk of pregnancy related venous thromboembolism (VTE), including deep vein thrombosis (DVT) and pulmonary embolism (PE). Pregnancy is a hypercoagulable state due to the increased concentration of coagulation factors, decreased natural anticoagulants and fibrinolytic activity1. The pregnant woman is therefore at increased risk for VTE and this ...
متن کاملThrombophilic Disorders in Migraine
Migraine is a widespread disorder that affects about 18% of the people, in 2/3 of cases women (1). The concept that migraine could be related to some vascular diseases, such as myocardial infarction or a stroke, have grown over the years, mainly in migraine with aura (2–6). In the last decades, several studies have been carried out to understand if and what the linkage could be. Among these stu...
متن کاملHereditary and acquired thrombophilic disorders complicating vascular access in haemodialysis
A 65-year-old male pre-dialysis Turkish patient with diabetic nephropathy received a Cimino fistula of the left lower arm, which occluded before use within the following weeks after the operation. A polytetrafluorethylene (PTFE) loop was created at the left forearm. The first sessions of dialysis were successful; however, 2 weeks after starting dialysis using unfractionated heparin, the loop oc...
متن کاملRole of Investigating Thrombophilic Disorders in Young Stroke
Our knowledge about various inherited and acquired causes of thrombophilic disorders has increased significantly during the past decade. Technology for various diagnostic tests for these rare disorders has matched the rapid advances in our understanding about the thrombophilic disorders. Inherited thrombophilic disorders predispose young patients for various venous or arterial thrombotic and th...
متن کامل[Thrombophilic disorders in children and adolescents with portal vein thrombosis].
OBJECTIVE To determine the frequency of protein C, protein S and antithrombin deficiency, and factor V Leiden, prothrombin G20210A, and methylenetetrahydrofolate reductase C677T mutations in children and adolescents with portal vein thrombosis, as well as assessing the hereditary character of this disorders. METHODS A two-year study was carried out to determine the frequency of thrombophilic ...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Laboratory Medicine
سال: 2001
ISSN: 1943-7730,0007-5027
DOI: 10.1309/45ky-0ajb-1t2h-x7cj