X-linked agammaglobulinemia (XLA), also known as Bruton's agammaglobulinemia, is a rare primary immunodeficiency characterized by an almost complete absence of mature B lymphocytes and immunoglobulins…
WHIM syndrome (Warts, Hypogammaglobulinemia, Infections, and Myelokathexis) is a rare, autosomal dominant primary immunodeficiency disorder caused primarily by gain-of-function mutations in the CXCR4 gene. It…
Hypogammaglobulinemia is an immunodeficiency disorder characterized by abnormally low levels of immunoglobulins, increasing susceptibility to recurrent bacterial infections. This condition can be primary (genetic) or…
Common Variable Agammaglobulinemia (CVA) is a primary immunodeficiency disorder characterized by a significant reduction or absence of immunoglobulins (antibodies) in the bloodstream. This condition leads…