vascular hemophilia; vascular pseudohemophilia; von Willebrand disease; von Willebrand disorder; von Willebrand’s-Jurgens’ disease; von Willebrand-Jrgens. The activity of vWF in a patient with von Willebrand disease. Aktywość vWF u pacjenta z chorobą Willebranda. Fig. 4. The activity of vWF in a. Hereditary bleeding disorders, such as von Willebrand disease, may be one of the causes of Choroba von Willebranda u kobiet z krwotocznymi miesiaczkami.
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Von Willebrandova choroba
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von Willebrand’s disease – Wikidata
Symptoms Skin Bruising Rectal bleeding not explained by a known source peptic ulcer, Colon PolypHemorrhoid Severe Anemia requiring transfusion Recurrent or persistent Epistaxis Bleeding lasting longer than willebranxa minutes or required medical attention Excessive bleeding with minor procedures e.
Evaluation Indications Personal or Family History of significant bleeding see symptoms as above and Planned for surgical procedure with moderate to high risk of bleeding or Current bleeding symptoms or abnormal lab results Complete history and examination See Choriba Disorder Symptoms suggestive of Bleeding Diathesis as listed above Medication causes of Bleeding Disorder e.
Differential Diagnosis See Bleeding Disorder. Related links to external sites from Bing. They are usually inherited as an autosomal dominant trait though rare kindreds are autosomal recessive.
Symptoms vary depending on severity and disease type but may include prolonged bleeding time, deficiency of factor VIII, and impaired platelet adhesion. The latter plays an important role bon platelet adhesion.
Signs and symptoms include bruises, nose bleeding, gum bleeding following a dental procedure, heavy menstrual bleeding, and gastrointestinal bleeding. Related Topics in Coagulopathy.
Hematology and Oncology Chapters. Hematology and Oncology – Coagulopathy Pages.
Von Willebrand disease – Wikipedia
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Includes true von Willebrand disease with mutation at the VWF locus, as well as mimicking disorders with other mutations pseudo VWD and acquired von Willebrand syndrome. Hereditary or acquired coagulation disorder characterized by a qualitative or quantitative deficiency of the von Willebrand factor. Disease or Syndrome T