Factor X Deficiency

What is a Factor X Deficiency?

Congenital factor X deficiency is an autosomal recessive inherited bleeding disorder caused by genetic defects on chromosome 13, resulting in a deficiency of factor X. Mildly affected individuals may have no symptoms but, in more severe cases, patients may experience hemorrhagic symptoms, such as nose bleeds or bleeding into the joints or muscles. Factor X deficiency can also be acquired as a result of liver disease, vitamin K deficiency or due to anticoagulants such as warfarin.

Resources for you

RESOURCE DESCRIPTION
All About Bleeding Information and resources to help treat and manage life with a bleeding disorder. View Website
  All About Bleeding Discussion guides View Website
Signs of Bleeding The 5 signs of a bleeding disorder View Website
World Federation of Hemophilia A global organization aiming to improve and sustain care for people with inherited bleeding disorders.
View Website
National Hemophilia Foundation A U.S. organization dedicated to finding better treatments and cures for inheritable bleeding disorders.
View Website
Hemophilia Federation of America A U.S. a national nonprofit organization that assists and advocates for the bleeding disorders community.
View Website

Treatments Available

Availability of treatments may vary from country to country. Please be sure to visit your local CSLBehring.com site for further information.

Factor X P Behring 
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