Laws H J, Harbrecht U, Köster B
Zentrum für Kinder- und Jugendmedizin des Kreiskrankenhauses Lüdenscheid.
Klin Padiatr. 1992 Nov-Dec;204(6):453-4. doi: 10.1055/s-2007-1025388.
Hereditary Factor VII deficiency is one of the rare congenital coagulopathies. Prolonged prothrombin time (PT) with normal partial prothrombin time (PTT) may be an indicator for Factor VII deficiency. A family with hereditary heterozygous Factor VII deficiency is presented in whom no symptoms of a bleeding disorder were clinically detectable. A discussion of the therapeutic options follows.