+ Site Statistics
+ Search Articles
+ PDF Full Text Service
How our service works
Request PDF Full Text
+ Follow Us
Follow on Facebook
Follow on Twitter
Follow on LinkedIn
+ Subscribe to Site Feeds
Most Shared
PDF Full Text
+ Translate
+ Recently Requested

Congenital factor VII -deficiency as a cause of a hemophilia-like hemorrhagic diathesis

Congenital factor VII -deficiency as a cause of a hemophilia-like hemorrhagic diathesis

Acta Haematol 16(3): 181-198

In a case of congenital factor VII-deficiency with a plasma content of 1.2% there was a relatively moderate tendency to hemorrhage. It is concluded, that Christmas-factor and factor VII are not identical, and that factor VII is not essential for the formation of thromboplastin in the blood in the early stages of clotting.

Please choose payment method:

(PDF emailed within 1 workday: $29.90)

Accession: 024382914

Download citation: RISBibTeXText

Related references

Angio-hemophilia A and B: nonhemophilic hemorrhagic diathesis with congenital deficiency of antihemophilic globulin-(factor IX). Folia Haematologica; Internationales Magazin für Blutforschung 1(3): 251-267, 1957

Isolated congenital factor V deficiency as cause of hemorrhagic diathesis. Wiener Zeitschrift für Innere Medizin und ihre Grenzgebiete 40(1): 10-16, 1959

A case of congenital hemorrhagic diathesis due to factor VII deficiency (hypoproconvertinemia). Wiadomosci Lekarskie 23(8): 661-664, 1970

Hemorrhagic diathesis caused by a congenital deficiency of a new coagulation factor (Prower-Stuart factor). Helvetica Paediatrica Acta 12(3): 260-270, 1957

Congenital factor VII (SPCA) deficiency as the cause of hemophilic-type hemorrhagic diathesis. Acta Haematologica 16(3): 181-198, 1956

Congenital hemorrhagic diathesis with deficiency of factor XIII. A case report and a family study. Thrombosis et Diathesis Haemorrhagica 23(2): 340-346, 1970

Congenital hemorrhagic syndrome due to deficiency of a prothromboplastic plasma factor different from the antihemophilic factor; hemophilia B. Le Sang 24(6): 488-495, 1953

Patients with congenital hemorrhagic diathesis in kagoshima prefecture japan 1. hemophilia and related diseases. Medical Journal of Kagoshima University 31(4): 721-728, 1980

Hemorrhagic diathesis (pseudo hemophilia) due to an specific inhibitor of factor VIII. Prensa Medica Argentina 57(1): 21-29, 1970

A family with angiohemophilia A (vascular hemophilia); hereditary hemorrhagic diathesis with prolonged bleeding time & partial antihemophilic globulin deficiency. Thrombosis et Diathesis Haemorrhagica 1(2): 223-233, 1957

A hemorrhagic diathesis due to proaccelerin deficiency (congenital parahemophilia); a case report. Connecticut State Medical Journal 17(8): 664-666, 1953

Congenital deficiency of the fibrinolysis inhibitor alpha 2-antiplasmin as a cause of hemorrhagic diathesis. Nederlands Tijdschrift Voor Geneeskunde 132(4): 167-170, 1988

Use of the P.P.B. Preparation in the Treatment of Hemorrhagic Diathesis with Congenital Deficiency of Coagulation Factors. Polski Tygodnik Lekarski 18: 201-207, 1963

Factor 5 deficiency in hemorrhagic diathesis. Jour Amer Med Assoc 148(6): 462-463, 1952

Hemorrhagic diathesis due to factor VII deficiency. A.M.A. Archives of Internal Medicine 99(2): 280-284, 1957