Sponsored diagnostic testing programs for Congenital Neutropenia
Congenital Neutropenia is a group of inherited disorders characterized by chronically low neutrophil counts, leading to recurrent bacterial infections, impaired immune defense, and, in some forms, an increased risk of bone marrow failure or leukemia. Severity and onset vary by subtype.
2 programs found for Congenital Neutropenia
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.
