Common variable immunodeficiency (CVID) is an antibody deficiency that leaves a child’s immune system vulnerable to recurrent infections, autoimmune diseases, lympho-proliferation and cancer. This is one of the most common forms of primary immunodeficiency disease, and severity varies from person to person.
Conditions We Treat
DiGeorge Syndrome (DGS) or 22q11.2 Deletion Syndrome is a primary immunodeficiency disease due to chromosome 22 deletion. Learn about symptoms & treatment.
Hyper IgM (HIGM) syndrome is a rare immune disorder in which a child's body doesn't produce certain disease-fighting antibodies.
Primary immunodeficiency disease (PIDD) is a group of more than 150 rare hereditary disorders in which the common feature is a defect in a patient's immune system.
Severe Combined Immunodeficiency (SCID) is the result of several defective genes in a child's immune system.
X-Linked Agammaglobulinemia (XLA) is an immune deficiency that affects Bruton's Tyrosine Kinase (BTK) & B-cells. Learn about XLA with Children's Health.
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