Glanzmann Thrombasthenia

Sponsored diagnostic testing programs for Glanzmann Thrombasthenia

Glanzmann Thrombasthenia is a rare inherited platelet function disorder caused by defects in the ITGA2B or ITGB3 genes. It leads to impaired platelet aggregation and results in easy bruising, frequent nosebleeds, and prolonged bleeding after injury or surgery.

1 program found for Glanzmann Thrombasthenia

Programs

1 program
Invitae Unlock™

Invitae Inborn Errors of Immunity and Cytopenias Panel

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.

Immunology