Autosomal recessive agammaglobulinaemia (Q102700): Difference between revisions

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Latest revision as of 19:54, 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
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.