Abstract
A patient with inherited combined deficiency of factor V and factor VIII is reported, who demonstrated normal levels of factor VIII antigen and plasma cofactor for ristocetin-induced platelet aggregation. The relationship of this condition to classical hemophilia and von Willebrand's disease is discussed. The data presented suggest that multiple loci on at least 2 chromosomes are necessary for the normal expression of factor VIII activity.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 385-391 |
| Number of pages | 7 |
| Journal | American Journal of Hematology |
| Volume | 2 |
| Issue number | 4 |
| DOIs | |
| State | Published - 1977 |
Keywords
- blood coagulation disorders
- factor V deficiency
- hemophilia
ASJC Scopus subject areas
- Hematology
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