Factor X deficiency--a rare disorder.

Abstract excerpt

Congenital factor X deficiency is a very rare inherited coagulation disorder. The clinical phenotype is of varying bleeding manifestations depending upon the level of factor activity. We describe a one and a half year old patient with severe deficiency (factor level less than 1%) who manifested with only easy bruisability and epistaxis that does not correlate with level of deficiency.

Topics

Share this publication in a Topic to start or enrich a Post.

• Share to Blood Coagulation Tests
• Share to Infant
• Share to Phenotype