Hemophilia is a genetically inherited bleeding disorder. There are two types of hemophilia: hemophilia A, or clotting factor VIII deficiency, and hemophilia B, or clotting factor IX deficiency. The degree of deficiency varies from mild to severe. About one third of hemophilia cases occur with no previous family history; this is called sporadic hemophilia. It is assumed that these cases are the result of genetic mutation.
An overview of the causes, symptoms and treatment of this blood disorder.
Information in note form for clinicians.
Committed to improve the quality of life of people affected by hemophilia and related blood conditions. Includes information, programs, regions, how to support the organization or volunteer.
Information on the signs, symptoms, causes and treatments of hemophilia A and B.
Multimedia guide where you can learn about this disease, what causes it, what it is like to have it, and how it is inherited, diagnosed, and treated.
Informational site for those with hemophilia and inhibitors.
This page is dedicated to my son, who has hemophilia.
Global hemophilia network for people suffering with this incurable bleeding disorder.
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