Definition of von Willebrand's disease in English:

von Willebrand's disease

nounˈwɪləbrandvän ˈviləbränts dəˌzēz

mass nounMedicine

An inherited disorder characterized by a tendency to bleed, caused by deficiency or abnormality of a plasma coagulation factor (von Willebrand factor).
〔医〕冯·维勒布兰德氏病
Example sentencesExamples
- The most commonly encountered disorders are coagulation factor VIII deficiency, coagulation factor IX deficiency and von Willebrand's disease.
- Bloat, epilepsy and heart related problems are also reported, as are von Willebrand's disease and hemophilia A.
- There is also impairment of the platelet response to thrombin, collagen, fibrinogen, and von Willebrand factor.
- Patients with Type 3 (and some with Type 2A and 2B) will need treatment with humate p, a medication derived from human plasma that contains both factor VIII and von Willebrand factor.
- In most patients with von Willebrand disease, factor VIII activity and plasma levels of von Willebrand factor are decreased.

Origin

1940s: named after Erik A. von Willebrand (1870–1949), Finnish physician.

Definition of von Willebrand's disease in US English:

von Willebrand's disease

nounvän ˈviləbränts dəˌzēz

Medicine

An inherited disorder characterized by a tendency to bleed, caused by deficiency or abnormality of a plasma coagulation factor (von Willebrand factor).
〔医〕冯·维勒布兰德氏病
Example sentencesExamples
- Patients with Type 3 (and some with Type 2A and 2B) will need treatment with humate p, a medication derived from human plasma that contains both factor VIII and von Willebrand factor.
- The most commonly encountered disorders are coagulation factor VIII deficiency, coagulation factor IX deficiency and von Willebrand's disease.
- In most patients with von Willebrand disease, factor VIII activity and plasma levels of von Willebrand factor are decreased.
- Bloat, epilepsy and heart related problems are also reported, as are von Willebrand's disease and hemophilia A.
- There is also impairment of the platelet response to thrombin, collagen, fibrinogen, and von Willebrand factor.

Origin

1940s: named after Erik A. von Willebrand (1870–1949), Finnish physician.

词汇	von Willebrand's disease
释义	Definition of von Willebrand's disease in English: von Willebrand's disease nounˈwɪləbrandvän ˈviləbränts dəˌzēz mass nounMedicine An inherited disorder characterized by a tendency to bleed, caused by deficiency or abnormality of a plasma coagulation factor (von Willebrand factor). 〔医〕冯·维勒布兰德氏病 Example sentencesExamples The most commonly encountered disorders are coagulation factor VIII deficiency, coagulation factor IX deficiency and von Willebrand's disease. Bloat, epilepsy and heart related problems are also reported, as are von Willebrand's disease and hemophilia A. There is also impairment of the platelet response to thrombin, collagen, fibrinogen, and von Willebrand factor. Patients with Type 3 (and some with Type 2A and 2B) will need treatment with humate p, a medication derived from human plasma that contains both factor VIII and von Willebrand factor. In most patients with von Willebrand disease, factor VIII activity and plasma levels of von Willebrand factor are decreased. Origin 1940s: named after Erik A. von Willebrand (1870–1949), Finnish physician. Definition of von Willebrand's disease in US English: von Willebrand's disease nounvän ˈviləbränts dəˌzēz Medicine An inherited disorder characterized by a tendency to bleed, caused by deficiency or abnormality of a plasma coagulation factor (von Willebrand factor). 〔医〕冯·维勒布兰德氏病 Example sentencesExamples Patients with Type 3 (and some with Type 2A and 2B) will need treatment with humate p, a medication derived from human plasma that contains both factor VIII and von Willebrand factor. The most commonly encountered disorders are coagulation factor VIII deficiency, coagulation factor IX deficiency and von Willebrand's disease. In most patients with von Willebrand disease, factor VIII activity and plasma levels of von Willebrand factor are decreased. Bloat, epilepsy and heart related problems are also reported, as are von Willebrand's disease and hemophilia A. There is also impairment of the platelet response to thrombin, collagen, fibrinogen, and von Willebrand factor. Origin 1940s: named after Erik A. von Willebrand (1870–1949), Finnish physician.
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