Immunodeficiency due to selective anti-polysaccharide antibody deficiency (Q88856): Difference between revisions
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13 August 2026
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Latest revision as of 15:14, 15 August 2026
Immunodeficiency due to selective anti-polysaccharide antibody deficiency is characterised by normal immunoglobulin levels (including IgG sub-classes) but impaired polysaccharide responsiveness (IPR). This syndrome is a rare primary immunodeficiency characterised by recurrent bacterial infections, mostly of the respiratory tract. The offending bacteria are those with a polysaccharide capsule, such as pneumococci, Hemophilus influenzae, meningococci and group B streptococci.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_849949348 |
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| English | Immunodeficiency due to selective anti-polysaccharide antibody deficiency |
Immunodeficiency due to selective anti-polysaccharide antibody deficiency is characterised by normal immunoglobulin levels (including IgG sub-classes) but impaired polysaccharide responsiveness (IPR). This syndrome is a rare primary immunodeficiency characterised by recurrent bacterial infections, mostly of the respiratory tract. The offending bacteria are those with a polysaccharide capsule, such as pneumococci, Hemophilus influenzae, meningococci and group B streptococci. |
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CID11:ID_849949348
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dki-india-ID_849949348
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Concluído
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13 August 2026
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