Clinical picture and treatment of 2212 patients with
common variable immunodeficiency.
Genetic approach to
common variable immunodeficiency and IgA deficiency.
Effect of regular intravenous immunoglobulin therapy on prevention of pneumonia in patients with
common variable immunodeficiency.
High serum levels of BAFF, APRIL, and TACT in
common variable immunodeficiency.
B-cell antibody defects account for around 50% of them, selective IgA deficiency being the most common, followed by
common variable immunodeficiency (CVI).
Lymphomas of mucosa-associated lymphoid tissue in
common variable immunodeficiency.
described a 54-year-old man with
common variable immunodeficiency and cirrhosis.
As shown in this table, 2 patients with IgG4 deficiency had severe infections and allergies; 1 patient with IgG3 deficiency had SLE and another had MBL deficiency; 1 patient with low IgG2 had pneumococcal pneumonia; 1 patient with low IgG 1 had Epstein-Barr virus infection and sepsis and later developed
common variable immunodeficiency after nine years of observation.
Background:
Common variable immunodeficiency (CVID) is one of the most common symptomatic primary immunodeficiency syndromes.
Common variable immunodeficiency (CVI) is a primary immunodeficiency characterized by hypogammaglobulinemia and an increased susceptibility to infections.
