Hereditary factor XI deficiency disease

Common Name(s)

Hereditary factor XI deficiency disease

Factor XI deficiency is an autosomal bleeding disorder characterized by reduced levels of factor XI in plasma (less than 15 IU/dL). Bleeding occurs mainly after trauma or surgery. On the basis of the concordance or discordance of F11 antigen and activity, the disorder is classified into the more frequent cross-reactive negative (CRM-) and the rarer CRM positive (CRM+) (summary by {9:Duga and Salomon, 2009}).
 

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Condition Specific Organizations

Following organizations serve the condition "Hereditary factor XI deficiency disease" for support, advocacy or research.

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Scientific Literature

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Clinical Trial Information This information is provided by ClinicalTrials.gov

The Proteins of the Contact Activation System
 

Status: Recruiting

Condition Summary: Factor XI Deficiency; Factor XII Deficiency

 

Last Updated: 30 May 2016

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