Chronic Granulomatous Disease (CGD) is a rare, inherited immunodeficiency disorder that affects the functioning of certain immune cells, leading to…
Wiskott-Aldrich Syndrome (WAS) is a rare genetic disorder that primarily affects males. It's characterized by a triad of symptoms: immunodeficiency,…
Hyper-IgM Syndrome in children is a rare genetic disorder characterized by an inability to effectively switch from the production of…
DiGeorge Syndrome, also known as 22q11.2 deletion syndrome, is a disorder caused by a defect in chromosome 22, resulting in…
X-linked Agammaglobulinemia (XLA) in children is a rare and serious primary immunodeficiency disease. Since it's genetically inherited and primarily affects…
Common Variable Immunodeficiency (CVID) is a disorder characterized by an impaired ability to produce antibodies, leading to a higher susceptibility…
Severe Combined Immunodeficiency (SCID) in children is a critical condition as they are born with very little or no immune…