Below you will find more information about Von Willebrand Disease from Medigest. If you believe that you are suffering from any of the symptoms of Von Willebrand Disease it is important that you obtain an accurate diagnosis from a medical professional to ensure that you obtain the correct medication or treatment for your condition. There are medical conditions that carry similar symptoms associated with Von Willebrand Disease and therefore the information provided by Medigest is offered as a guideline only and should never be used in preference to seeking professional medical advice. The information relating to Von Willebrand Disease comes from a third party source and Medigest will not be held liable for any inaccuracies relating to the information shown.
Von Willebrand Disease or VWD for brevity, is a common hereditary bleeding disorder. It is a coagulation abnormality which can be acquired as a result of medical conditions.
Diagnosis includes complete blood counts especially of the platelet, activated partial thromboplastin time or the APTT, Testing for factor IX are also performed if Hemophilia B is suspected.
Treatment includes no regular treatment however, prophylactic treatment is often given to patients with this kind of medical condition who are scheduled for surgery. It can also be treated with human derived medium purity factor VIII. Desmopressin is also administered to person with mild VWD.
Symptoms and Signs
Von Willerbrand Disease is usually without symptoms or asymptomatic however, it may be manifest through the occurrence of manifestations which include varying degree of bleeding. Usually bruising, bleeding of the nose and unusual blood loss during childbirth, among others is often seen with person with this medical condition. In addition, women who have this kind of disease experience heavy menstrual flows during menstruation period.
It is commonly caused by an alteration that adversely affects the person's platelets functioning as well as clotting (Fleisher,G. (2002). Synopsis of Pediatric Emergency Medicine, Lippincott Williams and Wilkins, p. 213).Discuss Von Willebrand Disease in our forums
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