PRIMARY IMMUNODEFICIENCES are usually referred to by the following -

"Common Variable Immunodeficiency",

"CVID",

"Hypogammaglobulinaemia",

"Agammaglobulinaemia",

"Severe Combined Immunodeficiency",

"SCID",

"X-linked SCID",

"Neutropenia",

"Hereditary Angioedema",

"HAE",

"X-linked agammaglobulinaemia",

"Bruton's Disease",

"XLA",

"Good's Syndrome"

"Wiskott-Aldrich Syndrome",

"IgG sub-classes",

"IgA deficiency",

"Hyper IgM",

"Selective IgA deficiency",

"Selective IgG sub-class deficiences",

"X-linked Lymphoproliferative Syndrome",

"Duncan's Syndrome",

"C1 esterase inhibitor deficiency",

"Hyper IgE Syndrome",

"Job's Syndrome".

This list may not include all possibilities.

If you can't find the information you need about any of these conditions on this website, especially from the "publications" section, please e-mail us at info@pia.org.uk and we will try to help you.