Immunodeficiency due to selective anti-polysaccharide antibody deficiency (Q88856): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed label, description and/or aliases in pt-br, en |
Changed an Item |
||
| Property / Canonical URI | |||
| Property / Canonical URI: https://id.who.int/icd/entity/849949348 / rank | |||
Normal rank | |||
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. |
