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Factor XI Mutation
You need to provide
Blood
This test is for
Male, Female
Test Preparation
Overview
What is Factor XI Mutation?
This test detects the deficiency in factor XI protein involved in blood clotting. A mutation in F11 gene results in deficiency of Factor XI which leads to abnormal blood clotting and this condition is known as Haemophilia C and Rosenthal syndrome. This test is recommended in case of symptoms such as frequent nosebleeds, easy bruising, bleeding under the skin and gums, prolonged bleeding after trauma or surgery, especially inside the oral cavity, nasal cavities or the urinary tract. This is a genetic disorder and can be inhereted as well.
Why is Factor XI Mutation done?
- When symptoms of bleeding disorder appear including excessive unexplained bleeding or excessive blood clotting
- When abnormal results appear in screening tests for coagulation factors
- For patients who have a family history of being diagnosed by a bleeding disorder
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