Sponsored diagnostic testing programs for Hyper IgM Syndrome
Hyper IgM Syndrome is a primary immunodeficiency characterized by normal or elevated IgM levels with markedly reduced IgG, IgA, and IgE due to impaired class-switch recombination. Patients are prone to recurrent bacterial infections, opportunistic infections, and may develop complications affecting the liver, blood, or gastrointestinal tract.
2 programs found for Hyper IgM Syndrome
Invitae Unlock™ Immunology provides clinicians with a comprehensive gene panel to evaluate patients with suspected primary immunodeficiency or immune-regulatory disorders. This no-charge program supports diagnostic clarification, aids in variant-guided care decisions, and can inform family cascade testing when appropriate.
Invitae Unlock Immunology offers sponsored access to the Inborn Errors of Immunity and Cytopenias Panel, Invitae’s most comprehensive assay for evaluating inherited immune disorders and cytopenias. The panel includes genes tied to combined immunodeficiencies, immune dysregulation, and bone marrow failure, supporting clearer diagnosis and management. U.S. providers may order for eligible patients.
