Autosomal recessive agammaglobulinaemia (Q102700): Difference between revisions
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Agamaglobulinemia autossômica é uma deficiência imunológica primária caracterizada por uma completa falta de células B maduras circulantes, resultando em agamaglobulinemia levando a uma suscetibilidade particular a infecções bacterianas dos tratos respiratório e digestivo. A meningoencefalite enteroviral é uma complicação muito grave e comum. | |||
| description / en | description / en | ||
Autosomal agammaglobulinemia is a primary immune deficiency characterised by a complete lack of circulating mature B cells, resulting in agammaglobulinemia leading to particular susceptibility to bacterial infections of the respiratory and digestive tracts. Enteroviral meningo-encephalitis is a very severe and not infrequent complication. | |||
Revision as of 19:53, 16 August 2026
Autosomal agammaglobulinemia is a primary immune deficiency characterised by a complete lack of circulating mature B cells, resulting in agammaglobulinemia leading to particular susceptibility to bacterial infections of the respiratory and digestive tracts. Enteroviral meningo-encephalitis is a very severe and not infrequent complication.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1395443519 |
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| English | Autosomal recessive agammaglobulinaemia |
Autosomal agammaglobulinemia is a primary immune deficiency characterised by a complete lack of circulating mature B cells, resulting in agammaglobulinemia leading to particular susceptibility to bacterial infections of the respiratory and digestive tracts. Enteroviral meningo-encephalitis is a very severe and not infrequent complication. |
