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Primære antistofmangelsyndromer

Forfatter(e)
Carsten Schade Larsen1, 2 & Terese L. Katzenstein3, 4 1) International Center of Immunodeficiency Diseases, Aarhus Universitetshospital 2) Infektionsmedicinsk Afdeling, Aarhus Universitetshospital 3) Infektionsmedicinsk Klinik, Rigshospitalet 4) Institut for Klinisk Medicin, Det Sundhedsvidenskabelige Fakultet, Københavns Universitet. Ugeskr Læger 2018;180:V07170549
Reference: 
Ugeskr Læger 2018;180:V07170549
Blad nummer: 
Sidetal: 
2-6
Primary antibody deficiency syndromes
Primary antibody deficiency syndromes (PAD) are a group of primary immunodeficiencies (PID) characterised by reduced production of immunoglobulins and recurrent respiratory tract infections. PAD varies from rare but life-threatening agammaglobulinaemias to frequent but often asymptomatic conditions such as selective IgA deficiency or IgG subclass deficiency. Common variable immunodeficiency is the clinically most important PAD. Hypogammaglobulinaemia may be associated with other PID or may be drug-induced or caused by infectious diseases, haematological malignancies or protein loss.
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