Sponsored diagnostic testing programs for Familial Hemophagocytic Lymphohistiocytosis (FHL) and Related Disorders
Familial Hemophagocytic Lymphohistiocytosis (FHL) is a severe inherited immune dysregulation disorder characterized by uncontrolled activation of immune cells, leading to persistent fevers, cytopenias, organ inflammation, and risk of life-threatening hyperinflammatory episodes. Symptoms typically appear in infancy or early childhood.
2 programs found for Familial Hemophagocytic Lymphohistiocytosis (FHL) and Related Disorders
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.
