Indication
Immunoglobulin deficiency
**Immunoglobulin deficiency** is a state of humoral immune dysfunction characterized by abnormally low serum levels of one or more antibody classes—such as IgG, IgA, or IgM—or an inability to produce functional specific antibodies. Read more about Immunoglobulin deficiency
4 drugs 1 manufacturers
Drugs that treat it
Common Immunoglobulin deficiency therapies.
GAMASTAN (immune globulin,gamma(IgG)/glycine)
GAMASTAN S-D (immune globulin,gamma(IgG)/glycine)
GAMASTAN S/D (immune globulin,gamma(IgG)/glycine)
News & literature
Coming soonRelated codes
Coming soonRelated conditions & guidelines
Coming soon**Immunoglobulin deficiency** is a state of humoral immune dysfunction characterized by abnormally low serum levels of one or more antibody classes—such as IgG, IgA, or IgM—or an inability to produce functional specific antibodies.
It can arise across all age groups as a primary, congenital inborn error of immunity—including common variable immunodeficiency or selective isotype deficiencies—or secondary to hematologic malignancies, protein-losing states, or immunosuppressive therapies.
Pathophysiologically, impaired B-cell maturation, plasma cell differentiation, or excessive antibody loss compromises humoral pathogen neutralization and opsonization.
Clinically, affected patients exhibit heightened susceptibility to recurrent, persistent, or severe sinopulmonary and gastrointestinal infections, predominantly caused by encapsulated bacteria, and face increased risks of bronchiectasis, autoimmune phenomena, and lymphoproliferative disorders.
- nih.gov
**Immunoglobulin deficiency** is a state of humoral immune dysfunction characterized by abnormally low serum levels of one or more antibody classes—such as IgG, IgA, or IgM—or an inability to produce functional specific antibodies Pathophysiologically, impaired B-cell maturation, plasma cell differentiation, or excessive antibody loss compromises humoral pathogen neutralization and opsonization
- nih.gov
**Immunoglobulin deficiency** is a state of humoral immune dysfunction characterized by abnormally low serum levels of one or more antibody classes—such as IgG, IgA, or IgM—or an inability to produce functional specific antibodies
- nih.gov
It can arise across all age groups as a primary, congenital inborn error of immunity—including common variable immunodeficiency or selective isotype deficiencies—or secondary to hematologic malignancies, protein-losing states, or immunosuppressive therapies Clinically, affected patients exhibit heightened susceptibility to recurrent, persistent, or severe sinopulmonary and gastrointestinal infections, predominantly caused by encapsulated bacteria, and face increased risks of bronchiectasis, auto...
- nih.gov
It can arise across all age groups as a primary, congenital inborn error of immunity—including common variable immunodeficiency or selective isotype deficiencies—or secondary to hematologic malignancies, protein-losing states, or immunosuppressive therapies Clinically, affected patients exhibit heightened susceptibility to recurrent, persistent, or severe sinopulmonary and gastrointestinal infections, predominantly caused by encapsulated bacteria, and face increased risks of bronchiectasis, auto...
- canadianallergyandimmunologytoday.com
It can arise across all age groups as a primary, congenital inborn error of immunity—including common variable immunodeficiency or selective isotype deficiencies—or secondary to hematologic malignancies, protein-losing states, or immunosuppressive therapies Pathophysiologically, impaired B-cell maturation, plasma cell differentiation, or excessive antibody loss compromises humoral pathogen neutralization and opsonization
- primaryimmune.org
Clinically, affected patients exhibit heightened susceptibility to recurrent, persistent, or severe sinopulmonary and gastrointestinal infections, predominantly caused by encapsulated bacteria, and face increased risks of bronchiectasis, autoimmune phenomena, and lymphoproliferative disorders
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