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Von Willebrand Disease

Diseases of the Blood and Immune Mechanism

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 System
Lymphatic or Immune System 1
ICD-10 Chapter
III: Diseases of the Blood and Blood-Forming Organs and Certain Disorders Involving the Immune Mechanism 1
Communicable or Non-communicable
Non-Communicable 2
Transmission Route
Non-Transmissible 3
First Described
1926 4
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 III
Quote, List of chapters, Chapter III
Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism
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2. Wikipedia: Non-communicable disease
WikipediaNamed examples section
Quote, 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.
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3. Wikipedia: Von Willebrand disease
WikipediaLead section, transmission-route statement
Quote, Lead section, transmission-route statement
It is the most common hereditary coagulopathy in humans, affecting 1% of the population.
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4. Von Willebrand Disease (Wikipedia)
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