Hemophilia

• Overview

  Hemophilia is an X-linked inherited bleeding disorder caused by mutation of the F8 or F9 gene Genetic analysis is useful for identification of the underlying genetic defect in males with severe, moderate or mild hemophilia and for determination of carrier status in the female individuals within their families.

• Approach

  Two algorithms for targeted diagnosis

  BloodCenter of Wisconsin provides a comprehensive menu of diagnostic tests for persons with hemophilia. This menu includes factor activity tests, factor inhibitor testing and comprehensive genetic testing.