Educational lecture on hereditary abnormalities of blood coagulation and thrombosis.
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چکیده
منابع مشابه
Thrombosis and coagulation abnormalities associated with cancer.
Abnormalities of hemostasis and malignancy have been recognized since the 19th century. Thrombosis and hypercoagulability are reported in as many as 60 percent of patients with malignancies. Decreased levels of protein coagulation factors, circulating anticoagulants and platelet numbers, and function changes are reported. The purpose of this work is to report a case of portal thrombosis in a pa...
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Clinical Implications of Acquired Blood Coagulation Abnormalities.
C OMPLEX ALTERATION of blood coagulation occurs in the course of a number of systemic disorders. In contrast to the congenital defects of hemnostasis which are usually characterized by a single clotting factor deficiency, the changes which may accompany acquired disease are characteristicallv multiple. These multiple defects tend to form typical patterns which reflect the physiologic abnormalit...
متن کاملfrequency of hereditary coagulation risk factors in deep vein thrombosis patients referred to iranian blood transfusion organization, kermanshah
introduction: the main inhibitors of coagulation pathway are antithrombin (at), protein c and protein s. these inhibitors are necessary to prevent thromboembolism. hereditary deficiency of inhibitors is the main cause of alteration in balance between the anti-clotting and the formation of thrombin. patients with this abnormality are susceptible to venous thromboembolism (vte). two major clinica...
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BACKGROUND Leprosy is a chronic dermato-neurological disease caused by Mycobacterium leprae infection. In 2016, more than 200,000 new cases of leprosy were detected around the world, representing the most frequent cause of infectious irreversible deformities and disabilities. PRINCIPAL FINDINGS In the present work, we demonstrate a consistent procoagulant profile on 40 reactional and non-reac...
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ژورنال
عنوان ژورنال: Nihon Naika Gakkai Zasshi
سال: 1987
ISSN: 0021-5384,1883-2083
DOI: 10.2169/naika.76.1515