Congenital factor V deficiency
What is Congenital factor V deficiency?
Congenital factor V deficiency is an inherited bleeding disorder due to reduced plasma levels of factor V (FV) and characterized by mild to severe bleeding symptoms.
Other condition names
- Owren disease
- Parahemophilia
- Proaccelerin deficiency
Inheritance type
Autosomal recessive
Prevalence
- Europe: 1-9 in 1,000 000
Age of Onset
- All ages
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