Sponsored diagnostic testing programs for Monogenic Congenital Diarrhea
Monogenic Congenital Diarrhea refers to a group of rare, inherited disorders caused by single-gene defects that disrupt intestinal absorption and fluid balance. Affected infants typically present with severe, early-onset diarrhea that may lead to dehydration, malnutrition, and growth failure.
2 programs found for Monogenic Congenital Diarrhea
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.
