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.
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An overview of the causes, symptoms and treatment of this blood disorder.
Information in note form for clinicians.
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.
Informational site for those with hemophilia and inhibitors.
An overview of the causes, symptoms and treatment of this blood disorder.
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.
Information in note form for clinicians.
This page is dedicated to my son, who has hemophilia.
Information on the signs, symptoms, causes and treatments of hemophilia A and B.
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Last update:
October 2, 2019 at 6:35:04 UTC
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Regional: Europe: United Kingdom: England: Berkshire: Earley
- Recently edited by merlin1
- Recently edited by merlin1