Autosomal recessive agammaglobulinaemia (Q102700)

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.