Von Willebrand disease is a type of blood-clotting disorder. It is the most common hereditary coagulopathy in humans, affecting 1 percent of the population, and an acquired form of the disease can sometimes result from other medical conditions. Most people with the disease have no symptoms, and those who do usually have bleeding of varying intensity, including repeated bruising and nosebleeds.
Facts
Classification
Body SystemLymphatic or Immune System 1 ICD-10 ChapterIII: Diseases of the Blood and Blood-Forming Organs and Certain Disorders Involving the Immune Mechanism 1 Communicable or Non-communicable Transmission Route Causative Agent
Causative Agent (category) First Described Connections
Treated By
Fresh frozen plasma or factor concentrate transfusion is a standard treatment for bleeding episodes in von Willebrand disease.
Sources
1. Wikipedia: ICD-10
WikipediaList of chapters, Chapter IIIQuote, List of chapters, Chapter III
Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism
View the Source 2. Wikipedia: Non-communicable disease
WikipediaNamed examples sectionQuote, Named examples section
NCDs include Parkinson's disease, autoimmune diseases, strokes, heart diseases, cancers, diabetes, chronic kidney disease, osteoarthritis, osteoporosis, Alzheimer's disease, cataracts, and others.
View the Source 3. Wikipedia: Von Willebrand disease
WikipediaLead section, transmission-route statementQuote, Lead section, transmission-route statement
It is the most common hereditary coagulopathy in humans, affecting 1% of the population.
View the Source 4. Von Willebrand Disease (Wikipedia)
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