Sponsored diagnostic testing programs for Pulmonary Alveolar Proteinosis (PAP)
Pulmonary Alveolar Proteinosis (PAP) is a rare disorder characterized by the accumulation of surfactant within the alveoli, leading to impaired gas exchange. Symptoms include progressive shortness of breath, cough, and fatigue. Some forms are caused by genetic defects affecting surfactant production or immune cell function.
2 programs found for Pulmonary Alveolar Proteinosis (PAP)
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.
