August 18, 2020

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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These images are a random sampling from a Bing search on the term “Von Willebrand Disease. Search Bing for all related images.

Von Willebrandova choroba

Started inthis collection now contains interlinked topic pages divided into a tree of 31 specialty books and chapters. Content is updated monthly with systematic literature reviews and conferences.

Although access to this website is not restricted, the information willebeanda here is intended for use by medical providers. Patients should address specific medical concerns with their physicians.


Related Bing Images Extra: Epidemiology Prevalance estimated at 1. 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 10 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 Bleeding Disorder Symptoms suggestive of Bleeding Diathesis as listed above Medication causes of Bleeding Disorder e.

Von Willebrandova choroba – WikiSkripta

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 in 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.

Canine Von Willebrand’s Disease – Hemophilia in Dogs

Hematology and Oncology – Coagulopathy Pages. Back Links pages that link to this page.

Search other sites for choeoba Willebrand Disease’. 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