Complement Deficiency Panel

The Complement Deficiency Panel analyzes genes that are associated with complement disorders. Complement disorders are characterized by increased risk for certain infections, autoimmune disease, atypical hemolytic uremic syndrome, or recurrent episodes of angioedema. Given the clinical overlap between these conditions, comprehensive testing enables a more efficient evaluation of multiple conditions based on a single indication for testing. This test may establish a genetic diagnosis, which would eliminate the need for serial gene testing. A genetic diagnosis may guide medical management, enabling a clinician to determine the need for additional evaluations, screenings, and procedures.