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[Hereditary heterozygote factor VII deficiency].

作者信息

Laws H J, Harbrecht U, Köster B

机构信息

Zentrum für Kinder- und Jugendmedizin des Kreiskrankenhauses Lüdenscheid.

出版信息

Klin Padiatr. 1992 Nov-Dec;204(6):453-4. doi: 10.1055/s-2007-1025388.

Abstract

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.

摘要

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