Common variable immunodeficiency (CVID) is a heterogeneous disorder characterized by
hypogammaglobulinemia and increased susceptibility to recurrent bacterial infections. It is …

Abstract Hyper Immunoglobulin M syndrome (HIGM) is a rare primary immunodeficiency
disorder characterized by low or absent levels of serum IgG, IgA, IgE and normal or …

Objective: To present the genetic causes of patients with primary immune deficiencies (PIDs)
in Kuwait between 2004 and 2017. Methods: The data was obtained from the Kuwait …

Objective: To present the report from the Kuwait National Primary Immunodeficiency
Registry between 2004 and 2018. Methods: The patients were followed prospectively …

Purpose Diagnostic delay is a major problem concerning common variable
immunodeficiency (CVID). We aimed to determine the pattern of general practitioner (GP) …

Abstract Background: Hyper-immunoglobulin M (HIGM) syndrome is a rare heterogeneous
group of primary immunodeficiency disorders characterized by low or absent serum levels of …

Monozygotic twins provide a unique opportunity to better understand complex genetic
diseases and the relative contribution of heritable factors in shaping the immune system …

Abstract Purpose Hyper Immunoglobulin M (HIgM) syndrome is a heterogeneous group of
primary immunodeficiency disorders, characterized by recurrent infections and associated …

Background: Agammaglobulinemia is a primary immunodeficiency disorders (PID) which is
identified by increased susceptibility to the bacterial infections, significant low antibodies …

Background/objectives: hyper-IgM (HIGM) syndrome is characterized by normal to increased
serum IgM and very low or undetectable IgG, IgA, and IgE. HIGM (also known as class …