Types of Immunodeficiency Disorders:
A. Antibody Deficiencies:
1. Common Variable Immunodeficiency (CVID): CVID is one of the most common PIDs, characterized by reduced antibody production, leading to recurrent bacterial infections, particularly of the respiratory and gastrointestinal tracts.
2. Selective IgA Deficiency: This condition involves a deficiency or absence of IgA antibodies, making affected individuals prone to respiratory, gastrointestinal, and genitourinary infections.
B. T Cell Deficiencies:
1. Severe Combined Immunodeficiency (SCID): SCID is a severe form of PID characterized by impaired T cell function, leading to a lack of both cellular and humoral immunity. SCID is life-threatening and requires early diagnosis and intervention, such as hematopoietic stem cell transplantation.
2. DiGeorge Syndrome: DiGeorge syndrome results from incomplete development of the thymus and parathyroid glands, leading to T cell deficiencies and calcium metabolism disorders.
C. Phagocyte Deficiencies:
1. Chronic Granulomatous Disease (CGD): CGD is a PID characterized by impaired phagocyte function, particularly neutrophils, leading to recurrent bacterial and fungal infections. CGD is due to defects in the NADPH oxidase enzyme complex.
2. Leukocyte Adhesion Deficiency (LAD): LAD is a group of disorders caused by defects in leukocyte adhesion molecules, resulting in impaired migration of immune cells to sites of infection and delayed wound healing.
D. Complement Deficiencies:
1. Hereditary Angioedema (HAE): HAE is caused by deficiencies or dysfunctions in complement proteins, leading to episodes of severe swelling of various body parts.
2. Complement Component Deficiencies: Deficiencies in various complement proteins can lead to increased susceptibility to certain infections, particularly encapsulated bacteria.
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