Haemophilia C caused by deficiency in Factor XI[1]
Specialty
Haematology
Symptoms
Oral bleeding[2]
Causes
Deficiency of coagulation factor XI[1]
Diagnostic method
Prothrombin time[1]
Prevention
Physical activity precautions[1]
Treatment
tranexamic acid[3]
Haemophilia C (also known as plasma thromboplastin antecedent (PTA) deficiency or Rosenthal syndrome) is a mild form of haemophilia affecting both sexes, due to factor XI deficiency.[4] It predominantly occurs in Ashkenazi Jews. It is the fourth most common coagulation disorder after von Willebrand's disease and haemophilia A and B. In the United States, it is thought to affect 1 in 100,000 of the adult population, making it 10% as common as haemophilia A.[1][5]
^ abcde"Hemophilia C: Background, Etiology, Epidemiology". December 9, 2021 – via eMedicine. {{cite journal}}: Cite journal requires |journal= (help)
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^"Factor XI deficiency | Disease | Overview | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program". rarediseases.info.nih.gov. Archived from the original on 2019-12-16. Retrieved 2016-07-09.
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