Immunodeficiency due to selective anti-polysaccharide antibody deficiency (Q88856): Difference between revisions

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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
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.